| 100050 : AARSKOG SYNDROME 100070 : ABDOMINAL AORTIC ANEURYSM 100100 : ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY AND CRYPTORCHIDISM 100200 : ABDUCENS PALSY 100675 : ACETAMINOPHEN METABOLISM 100680 : ACETYLCHOLINESTERASE EXPRESSION; ACEE 100700 : ACHARD SYNDROME 101120 : ACROCEPHALOPOLYSYNDACTYLY TYPE III 101805 : ACROFACIAL DYSOSTOSIS, CATANIA TYPE 101840 : ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT 102000 : ACROLEUKOPATHY, SYMMETRIC 102370 : ACROMICRIC DYSPLASIA 102400 : ACROOSTEOLYSIS 102490 : ACRORENOOCULAR SYNDROME 102520 : ACRORENAL SYNDROME 102530 : ACROSOME MALFORMATION OF SPERMATOZOA 102590 : ACYLASE, COBALT-ACTIVATED 102650 : ADACTYLIA, UNILATERAL 102660 : ADAMANTINOMA OF LONG BONES 102699 : ADENO-ASSOCIATED VIRUS INTEGRATION SITE 1; AAVS1 102710 : ADENOSINE DEAMINASE COMPLEXING PROTEIN 1; ADCP1 102730 : ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO 102920 : ADENOVIRUS-12 CHROMOSOME MODIFICATION SITE 1A; A12M2 102930 : ADENOVIRUS-12 CHROMOSOME MODIFICATION SITE 1C; A12M1 102940 : ADENOVIRUS-12 CHROMOSOME MODIFICATION SITE 1B; A12M3 102970 : ADENOVIRUS-12 CHROMOSOME MODIFICATION SITE 17; A12M4 102990 : ADENYLATE KINASE, MUSCLE, DEFICIENCY OF 103100 : ADIE SYNDROME 103200 : ADIPOSIS DOLOROSA 103230 : ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL 103285 : ADULT SYNDROME 103300 : AGLOSSIA-ADACTYLIA 103400 : AINHUM 103581 : ALBRIGHT HEREDITARY OSTEODYSTROPHY 2; AHO2 103780 : ALCOHOLISM 103920 : ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS 104000 : ALOPECIA AREATA 104100 : ALOPECIA CONGENITA WITH KERATOSIS PALMOPLANTARIS 104110 : ALOPECIA, FAMILIAL FOCAL 104290 : ALTERNATING HEMIPLEGIA OF CHILDHOOD 104350 : AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM 104400 : AMELIA AND TERMINAL TRANSVERSE HEMIMELIA 104510 : AMELOGENESIS IMPERFECTA, HYPOMATURATION-HYPOPLASIA TYPE, WITH TAURODONTISM 104600 : AMENORRHEA-GALACTORRHEA SYNDROME 105300 : AMYOTROPHIC DYSTONIC PARAPLEGIA 105500 : AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX OF GUAM 105550 : AMYOTROPHIC LATERAL SCLEROSIS WITH DEMENTIA 105563 : ANAL SPHINCTER DYSPLASIA; ASDP 105565 : ANAL SPHINCTER MYOPATHY, INTERNAL 105570 : ANDROSTENONE, ABILITY TO SMELL 105580 : ANAL CANAL CARCINOMA 105805 : ANEURYSM OF INTERVENTRICULAR SEPTUM 105835 : ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA; ASPED 106050 : ANGIOMA SERPIGINOSUM 106160 : ANGIOTENSIN II BINDING PROTEIN 106190 : ANHIDROSIS, FAMILIAL GENERALIZED, WITH NORMAL SWEAT GLANDS 106220 : ANIRIDIA AND ABSENT PATELLA 106230 : ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT 106240 : ANISOCORIA 106250 : ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE 106260 : ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE 106280 : ANKYLOGLOSSIA 106400 : ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSIS 106500 : ANNULAR ERYTHEMA 106750 : ANONYCHIA WITH FLEXURAL PIGMENTATION 106900 : ANONYCHIA-ECTRODACTYLY 106990 : ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY 107000 : ANONYCHIA-ONYCHODYSTROPHY 107200 : ANOSMIA, CONGENITAL 107320 : ANTIPHOSPHOLIPID SYNDROME 107440 : ANTIVIRAL STATE REPRESSOR, REGULATOR OF; AVRR 107500 : AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION 107550 : AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA 107601 : APLASIA CUTIS CONGENITA AND COARCTATION OF AORTA; ACCCA 107640 : APNEA, CENTRAL SLEEP 107700 : APPENDICITIS, PRONENESS TO 107760 : APOLIPOPROTEIN F; APOF 107800 : ARCUS CORNEAE 107850 : ARM FOLDING PREFERENCE 107900 : ARMS, MALFORMATION OF 107920 : AROMATIC ALPHA-KETO ACID REDUCTASE 108000 : ARTERIES, ANOMALIES OF 108010 : ARTERIOVENOUS MALFORMATIONS OF THE BRAIN 108050 : ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS 108100 : ARTHRITIS, SACROILIAC 108110 : ARTHROGRYPOSIS MULTIPLEX CONGENITA; AMC 108130 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE II 108140 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE II, WITH CRANIOFACIAL ABNORMALITIES 108145 : ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES 108200 : ARTHROGRYPOSIS-LIKE HAND ANOMALY AND SENSORINEURAL DEAFNESS 108320 : ARTICHOKE, MODIFICATION OF TASTE BY 108390 : ASPARAGUS, SPECIFIC SMELL HYPERSENSITIVITY 108400 : ASPARAGUS, URINARY EXCRETION OF ODORIFEROUS COMPONENT OF 108420 : ASPERMIOGENESIS FACTOR; ASG 108450 : ASYMMETRIC SHORT STATURE SYNDROME 108700 : ATAXIA WITH FASCICULATIONS 108720 : ATELOSTEOGENESIS, TYPE I 108725 : ATHEROSCLEROSIS SUSCEPTIBILITY; ATHS 108770 : ATRIAL CARDIOMYOPATHY WITH HEART BLOCK 108950 : ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL 108970 : ATRIOPEPTIDASE 108980 : ATRIOVENTRICULAR CONDUCTION TIME 109050 : AUROCEPHALOSYNDACTYLY 109120 : AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES 109130 : AXIAL OSTEOMALACIA 109180 : BABOON M7 VIRUS INTEGRATION SITE; BEVI 109300 : BANKI SYNDROME 109350 : BARRETT ESOPHAGUS 109390 : BASAL CELL CARCINOMAS WITH MILIA AND COARSE, SPARSE HAIR 109500 : BASILAR IMPRESSION, PRIMARY 109540 : B-CELL GROWTH FACTOR; BCGF 109600 : BEETURIA 109650 : BEHCET SYNDROME 109670 : BETA-ADRENERGIC STIMULATION, RESPONSE TO; BAS 109720 : BILIARY CIRRHOSIS, PRIMARY; PBC 109730 : BICUSPID AORTIC VALVE 109740 : BIFID NOSE 109820 : BLADDER DIVERTICULUM 109900 : BLEPHAROCHALASIS AND DOUBLE LIP 110000 : BLEPHAROCHALASIS, SUPERIOR 110050 : BLEPHARONASOFACIAL MALFORMATION SYNDROME 110150 : BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS 110250 : BLOOD GROUPABO SUPPRESSOR 110310 : BLOOD GROUPABH ANTIGEN, TYPE 2 110720 : BLOOD GROUPEn 111360 : BLOOD GROUPNEWFOUNDLAND; NFLD 111620 : BLOOD GROUPRADIN ANTIGEN; Rd 112240 : BONE FRAGILITY WITH CRANIOSYNOSTOSIS, OCULAR PROPTOSIS, HYDROCEPHALUS, AND DISTINCTIVE FACIAL FEATURES 112270 : BONE PAIN, PERIODIC 112310 : BOOMERANG DYSPLASIA 112350 : BOWING OF LEGS, ANTERIOR, WITH DWARFISM 112370 : BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUS ADDUCTUS, AND DEVELOPMENTAL DELAY 112430 : BRACHYDACTYLY, LONG-THUMB TYPE 112440 : BRACHYDACTYLY, COMBINED B AND E TYPES 112450 : BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION 112910 : BRACHYDACTYLY, TYPE A6; BDA6 113301 : BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II 113310 : BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA 113400 : BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA 113450 : BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME 113470 : BRACHYMESOMELIA-RENAL SYNDROME 113475 : BRACHYMETATARSUS IV 113477 : BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME 113480 : BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME 113500 : BRACHYRACHIA 113600 : BRANCHIAL CLEFT ANOMALIES 113610 : BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA 113670 : BREAST, UNILATERAL GIANT 113700 : BREASTS AND NIPPLES, ABSENCE OF 113960 : BUTYRYLESTERASE 1 114065 : CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL 114078 : CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE II-ALPHA; CAMK2A 114100 : CALCIFICATION OF BASAL GANGLIA WITH OR WITHOUT HYPOCALCEMIA 114120 : CALCINOSIS, TUMORAL 114190 : CALCITONIN GENE-RELATED PEPTIDE RECEPTOR; CGRPR 114450 : CANCER, FAMILIAL, WITH IN VITRO RADIORESISTANCE 114580 : CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, DOMINANT TYPE 114620 : CANTU SYNDROME 114650 : CAR FACTOR DEFICIENCY 114700 : CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH 114900 : CARCINOID, INTESTINAL 115000 : CARDIAC ARRHYTHMIA 115198 : CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 5 115250 : CARDIOMYOPATHY-HYPOGONADISM-COLLAGENOMA SYNDROME 115300 : CAROTENEMIA, FAMILIAL 115310 : CAROTID BODY TUMORS AND MULTIPLE EXTRAADRENAL PHEOCHROMOCYTOMAS 115400 : CARPAL DISPLACEMENT 115645 : CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION 116100 : CATARACT, MEMBRANOUS 116700 : CATARACT, TOTAL CONGENITAL; CC 116850 : CATATRICHY 116870 : CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENT OF DIAPHRAGM 117300 : CEREBELLAR ATAXIA, CATARACT, DEAFNESS, AND DEMENTIA OR PSYCHOSIS 117360 : CEREBELLAR VERMIS APLASIA 117600 : CEREBRAL SARCOMA 117650 : CEREBROCOSTOMANDIBULAR SYNDROME 117850 : CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS 117900 : CERVICAL RIB 118000 : CERVICAL VERTEBRAL BRIDGE 118005 : CERVICAL VERTEBRAL DYSPLASIA 118230 : CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE 118301 : CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM 118330 : CHEILITIS GLANDULARIS 118350 : CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS 118420 : CHIARI MALFORMATION TYPE I 118430 : CHLORPROPAMIDE-ALCOHOL FLUSHING; CPAF 118610 : CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION 118651 : CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE 118670 : CHONDRONECTIN; CHN 118750 : CHOREOATHETOSIS, FAMILIAL INVERTED 118865 : CHOROIDAL OSTEOMA, BILATERAL 118900 : CIRRHOSIS, FAMILIAL 118943 : CHYMOSIN PSEUDOGENE; CYMP 118980 : CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL 119540 : CLEFT PALATE; CP 119570 : CLEFT SOFT PALATE 119580 : BLEPHAROCHEILODONTIC SYNDROME 119650 : CLEIDORHIZOMELIC SYNDROME 119800 : CLUBFOOT 119915 : CLUSTER HEADACHE, FAMILIAL 120000 : COARCTATION OF AORTA 120040 : COCHLEOSACCULAR DEGENERATION OF THE INNER EAR WITH PROGRESSIVE CATARACTS 120400 : COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY 120430 : COLOBOMA OF OPTIC NERVE 120433 : COLOBOMA, UVEAL, WITH CLEFT LIP AND PALATE AND MENTAL RETARDATION 120440 : COLONIC VARICES WITHOUT PORTAL HYPERTENSION 120450 : COMEDONES, FAMILIAL DYSKERATOTIC 120460 : COLORECTAL CANCER-RELATED CHROMOSOME SEQUENCE-17; CRCR2; CRC17 120500 : COMMISSURAL LIP PITS 120502 : COMMISSURAL LIP PITS WITH CONGENITAL CONDUCTIVE OR MIXED DEAFNESS, PREAURICULAR SINUS, AND EXTERNAL EAR ANOMALY 121020 : CONTINUOUS MUSCLE FIBER ACTIVITY, HEREDITARY 121070 : CONTRACTURES OF FINGERS AND JAW 121270 : COPPER DEFICIENCY, FAMILIAL BENIGN 121350 : CORACOCLAVICULAR JOINT, ANOMALOUS 121450 : CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS 121820 : CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE 122430 : CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS, UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION 122440 : CORNEODERMATOOSSEOUS SYNDROME 122455 : CORONARY ARTERY DISSECTION, SPONTANEOUS 122470 : CORNELIA DE LANGE SYNDROME 1; CDL1 122550 : CORTICOSTERONE SIDE-CHAIN ISOMERASE; CSCI 122580 : COSTOCORACOID LIGAMENT, CONGENITALLY SHORT 122780 : COXOAURICULAR SYNDROME 122850 : CRANIOACROFACIAL SYNDROME 122860 : CRANIODIAPHYSEAL DYSPLASIA, DOMINANT 122900 : CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA 122920 : CRANIOFRONTAL DYSPLASIA 123050 : CRANIORHINY 123155 : CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS 123270 : CREATINE KINASE, BRAIN TYPE, ECTOPIC EXPRESSION OF; CKBE 123320 : CREATINE PHOSPHOKINASE, ELEVATED SERUM 123540 : CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY 123557 : CRYPTOTIA, FAMILIAL 123560 : CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME 123853 : CYPRUS FACIAL NEUROMUSCULOSKELETAL SYNDROME 123880 : CYSTIC ANGIOMATOSIS OF BONE, DIFFUSE 124000 : CYTOCHROME-RELATED DISEASE OF MUSCLE AND NERVOUS SYSTEM 124100 : DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY 124300 : DARWINIAN POINT OF PINNA 124400 : DARWINIAN TUBERCLE OF PINNA 124490 : DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY 124580 : DEAFNESS, DOMINANT CONGENITAL SEVERE SENSORINEURAL 124910 : DEAFNESS: LOW-FREQUENCY HEARING LOSS, MIXED CONDUCTIVE-SENSORINEURAL TYPE 124950 : DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE 125000 : DEAFNESS, UNILATERAL 125050 : DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA 125100 : DEAFNESS WITH EAR PITS 125230 : DEAFNESS-CRANIOFACIAL SYNDROME 125250 : DEAFNESSOPTIC ATROPHY SYNDROME 125280 : DENS EVAGINATUS 125300 : DENS IN DENTE AND PALATAL INVAGINATIONS 125320 : DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES 125350 : DENTAL NONERUPTION 125460 : DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY 125500 : DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III 125510 : DEPRESSIVE DISEASE, PURE 125530 : DERMAL RIDGES, NELSON SYNDROME 125570 : DERMATOGLYPHICSARCH ON ANY DIGIT 125580 : DERMATOGLYPHICSFINGER RIDGE COUNT 125590 : DERMATOGLYPHICSFINGERPRINT PATTERN 125595 : DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR 125600 : DERMATOSIS PAPULOSA NIGRA 125630 : DERMODISTORTIVE URTICARIA; DDU 125635 : DERMOGRAPHISM, FAMILIAL 125640 : DERMOODONTODYSPLASIA 125890 : DIARRHEA, GLUCOSE-STIMULATED SECRETORY, WITH COMMON VARIABLE IMMUNODEFICIENCY 125900 : DIASTEMA, DENTAL MEDIAL 126100 : DIMPLES, FACIAL 126180 : DISCRIMINATION, TWO-POINT, REDUCTION IN 126190 : DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS 126200 : MULTIPLE SCLEROSIS; MS 126250 : DISTAL OSTEOSCLEROSIS 126320 : DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL VASCULATURE 126370 : DNA, SATELLITE, III; HS3; D1Z1 126390 : DNA, LOW-REPETITIVE SEQUENCES OF 126410 : DNA, SATELLITE, ALPHA TYPE 126440 : DNA G-T MISMATCH REPAIR PROTEIN p200 126448 : DOPAMINE RECEPTOR D1B 126500 : DOUBLE NAIL FOR FIFTH TOE 126550 : DOUGHNUT LESIONS OF SKULL, FAMILIAL 126700 : DRUSEN OF BRUCH MEMBRANE 126830 : DUCK-BILL LIPS AND PTOSIS 126840 : DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION 126950 : DWARFISM WITH TALL VERTEBRAE 127100 : DWARFISM, LEVI TYPE 127200 : DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES 127350 : DYSCHONDROSTEOSIS AND NEPHRITIS 127500 : DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 127550 : DYSKERATOSIS CONGENITA, SCOGGINS TYPE 127750 : LEWY BODY DEMENTIA 127800 : DYSPLASIA EPIPHYSEALIS HEMIMELICA 127820 : DYSPLASIA EPIPHYSEALIS HEMIMELICA WITH CHONDROMAS AND OSTEOCHONDROMAS 128290 : EAR ANTITRAGUS, TAG AT BASE OF 128300 : EAR EXOSTOSES 128400 : EAR FLARE 128500 : EAR FOLDING 128710 : EAR PITS, POSTERIOR HELICAL 128800 : EAR WITHOUT HELIX 128900 : EARLOBE ATTACHMENT: ATTACHED VS UNATTACHED 128950 : EARLOBE CREASE 129000 : EARRING HOLES, NATURAL 129100 : EARS, ABILITY TO MOVE 129510 : ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE 129540 : ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE AND PREAXIAL POLYDACTYLY OF FEET 129550 : ECTODERMAL DYSPLASIA WITH ADRENAL CYST 129810 : ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE 129830 : ECTRODACTYLY-CLEFT PALATE SYNDROME 129840 : EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL 129850 : EDINBURGH MALFORMATION SYNDROME 129905 : EGASYN 130020 : EHLERS-DANLOS SYNDROME, TYPE III 130070 : EHLERS-DANLOS SYNDROME, PROGEROID FORM 130090 : EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED 130100 : ELASTOSIS PERFORANS SERPIGINOSA; EPS 130200 : ELECTROENCEPHALOGRAPHIC PECULIARITY: 14 AND 6 PER SEC. POSITIVE SPIKE PHENOMENON 130300 : ELECTROENCEPHALOGRAPHIC PECULIARITY: FRONTO-PRECENTRAL BETA WAVE GROUPS 130400 : ELECTROENCEPHALOGRAPHIC PECULIARITY: OCCIPITAL SLOW BETA WAVES 130700 : EMPHYSEMA 130710 : EMPHYSEMA, CONGENITAL LOBAR; CLE 130720 : EMPTY SELLA TURCICA, PRIMARY, WITH GENERALIZED DYSPLASIA 130900 : ENAMEL HYPOPLASIA, HEREDITARY LOCALIZED 130950 : ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD 131200 : ENDOMETRIOSIS 131375 : ENOLASE, SPERM SPECIFIC; ENO4 131430 : EOSINOPHILOPENIA 131440 : EOSINOPHILS, MALIGNANT PROLIFERATION OF 131445 : EPENDYMOMA, FAMILIAL 131450 : EPIBLEPHARON OF LOWER LID 131460 : EPIBLEPHARON OF UPPER LID 131600 : EPIDERMOID CYSTS 131880 : EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE 132090 : EPILEPSY, BENIGN OCCIPITAL; BOE 132100 : EPILEPSY, PHOTOGENIC 132300 : EPILEPSY, READING 132500 : EPISTAXIS, HEREDITARY 132600 : EPITHELIOMA CALCIFICANS OF MALHERBE 132850 : EPSTEIN-BARR VIRUS INSERTION SITE 1; EBVS1 132860 : EPSTEIN-BARR VIRUS MODIFICATION SITE 1; EBVM1 132990 : ERYTHEMA NODOSUM, FAMILIAL 133020 : ERYTHERMALGIA, FAMILIAL PRIMARY 133180 : ERYTHROLEUKEMIA, FAMILIAL 133239 : ESOPHAGEAL CANCER 133240 : ESOPHAGEAL RING, LOWER 133260 : ESTERASE B; ESB 133270 : ESTERASE C; ESC 133300 : ESTERASE ES-2, REGULATOR FOR 133600 : EXOSTOSES OF HEEL 133690 : EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E 133705 : EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS 133750 : EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATION AND MICROCEPHALY 133800 : EYEBROW, WHORL IN 133900 : FACIAL ASYMMETRY 134000 : FACIAL HYPERTRICHOSIS 134100 : FACIAL PALSY, CONGENITAL UNILATERAL OR BILATERAL 134300 : FACIAL SPASM 134400 : FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS 134430 : FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF 134500 : FACTOR VIII DEFICIENCY 134510 : FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF 134520 : FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF 134530 : FACTOR X, QUANTITATIVE VARIATION IN 134540 : FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF 134632 : FARNESYL DIPHOSPHATE SYNTHASE-LIKE 2; FDPSL2 134633 : FARNESYLPYROPHOSPHATE SYNTHETASE 3; FPSL3 134634 : FARNESYLPYROPHOSPHATE SYNTHETASE 4; FPSL4 134700 : FAVISM, SUSCEPTIBILITY TO 134720 : FECUNDITY GENE, BOOROOLA, OF SHEEP, HOMOLOG OF; FECB 134750 : FELTY SYNDROME 134780 : FEMORAL-FACIAL SYNDROME; FFS 134900 : FIBRINOLYTIC DEFECT 135150 : FIBROFOLLICULOMAS WITH TRICHODISCOMAS AND ACROCHORDONS 135400 : FIBROMATOSIS, GINGIVAL, WITH HYPERTRICHOSIS 135580 : FIBROMUSCULAR DYSPLASIA OF ARTERIES 135610 : FIBRONECTIN-LIKE 2; FNL2 135750 : FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUS 135800 : FIBULA, RECURRENT DISLOCATION OF HEAD OF 135900 : FIFTH DIGIT SYNDROME 135950 : FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION AND PROPORTIONATE SHORT STATURE 136100 : FINGERS, RELATIVE LENGTH OF 136140 : FLOATING-HARBOR SYNDROME 136150 : FLOOD FACTOR DEFICIENCY 136200 : FLUSHING OF EARS AND SOMNOLENCE 136400 : FOCAL EPITHELIAL HYPERPLASIA OF THE ORAL MUCOSA 136470 : FOLLISTATIN 136480 : FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL 136600 : FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURAL DEAFNESS 136750 : FRIEND MURINE LEUKEMIA VIRUS INTEGRATION SITE 1, MOUSE, HOMOLOG OF; FIM1 136760 : FRONTONASAL DYSPLASIA 136770 : FRIEND MURINE LEUKEMIA VIRUS INTEGRATION SITE 3, MOUSE, HOMOLOG OF; FIM3 136830 : FUCOSIDASE REGULATOR 137000 : FUTCHER LINE 137030 : GALACTOSE + ACTIVATOR; GLAT 137040 : GALLBLADDER, AGENESIS OF 137050 : GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF 137130 : GASTRIC SNEEZING 137200 : GAMSTORP-WOHLFART SYNDROME 137210 : GASTRIC VOLVULUS, INTRATHORACIC 137220 : GASTRIC JUICE PEPTIDES 137245 : GASTRIC LYMPHOMA, PRIMARY 137270 : GASTROCUTANEOUS SYNDROME 137280 : GASTRITIS, FAMILIAL GIANT HYPERTROPHIC 137360 : GENOCHONDROMATOSIS 137370 : GENU VALGUM, ST. HELENA FAMILIAL 137400 : GEOGRAPHIC TONGUE AND FISSURED TONGUE 137550 : GIANT PIGMENTED HAIRY NEVUS; GPHN 137560 : GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA 137575 : GIGANTIFORM CEMENTOMA, FAMILIAL 137700 : GLAUCOMA WITH ELEVATED EPISCLERAL VENOUS PRESSURE 137763 : GLAUCOMA AND SLEEP APNEA 137765 : GLAUCOMA-LENS ECTOPIA-MICROSPHEROPHAKIA-STIFFNESS-SHORTNESS SYNDROME; GEMSS 137900 : GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN 137920 : GLOMERULOCYSTIC KIDNEY DISEASE, FAMILIAL; GCKD 137940 : GLOMERULONEPHRITIS WITH SPARSE HAIR AND TELANGIECTASES 137950 : GLOMERULOPATHY WITH GIANT FIBRILLAR DEPOSITS 138070 : GLUCOGLYCINURIA 138110 : GLUCOSE-6-PHOSPHATE DEHYDROGENASE-LIKE; G6PDL 138210 : GLUTAMATE-PYRUVATE TRANSAMINASE, MITOCHONDRIAL; GPT2 138277 : GLUTAMIC ACID DECARBOXYLASE, BRAIN, MEMBRANE FORM 138340 : GLUTATHIONE TRANSFERASE ACTIVITY TOWARD TRANS-STILBENE OXIDE 138391 : GLUTATHIONE S-TRANSFERASE 6 138500 : GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS 138710 : GLYCOPROTEIN, RENAL 138770 : GMS SYNDROME 138790 : GOITER, MULTINODULAR, CYSTIC RENAL DISEASE AND DIGITAL ANOMALIES 138900 : GOUT 138920 : GRANDDAD SYNDROME 138930 : GRANT SYNDROME 138972 : GRANULOCYTE COLONY-STIMULATING FACTOR PROMOTER ELEMENT-1, BINDING PROTEIN FOR; GPE1BP 138990 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL DOMINANT TYPE 139000 : GRANULOSIS RUBRA NASI 139210 : GROWTH-MENTAL DEFICIENCY SYNDROME OF MYHRE 139260 : GUANASE 139280 : GUANYLATE KINASE 2; GUK2 139300 : GYNECOMASTIA, HEREDITARY 139393 : GUILLAIN-BARRE SYNDROME, FAMILIAL 139395 : GUSTDUCIN, ALPHA POLYPEPTIDE 139400 : HAIR WHORL 139450 : HAIR, CURLY 139500 : HAIRY EARS 139600 : HAIRY ELBOWS 139630 : HAIRY NOSE TIP 139750 : HAND AND FOOT DEFORMITY WITH FLAT FACIES 139800 : HAND CLASPING PATTERN 139900 : HANDEDNESS 140300 : HASHIMOTO STRUMA 140450 : HEART-HAND SYNDROME, SPANISH TYPE 140500 : HEART, MALFORMATION OF 140600 : HEBERDEN NODES 140850 : HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE 140900 : HEMANGIOMAS OF SMALL INTESTINE 141000 : HEMANGIOMA-THROMBOCYTOPENIA SYNDROME 141300 : HEMIFACIAL ATROPHY, PROGRESSIVE; HFA 141400 : HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS 141405 : HEMIFACIAL SPASM, FAMILIAL 141700 : HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES 142270 : HEMOGLOBINGAMMA, REGULATOR OF; HBGR 142330 : HEPATIC ADENOMAS, FAMILIAL 142333 : HEPATITIS B VIRUS INTEGRATION SITE 7; HVBS7 142340 : HERNIA, DIAPHRAGMATIC 142350 : HERNIA, DOUBLE INGUINAL 142395 : HEPATITIS B VACCINE, RESPONSE TO 142400 : HERNIA, HIATUS 142420 : HERPES SIMPLEX VIRUS-1 INTEGRATION SITE 142500 : HETEROCHROMIA IRIDIS 142550 : HEXOKINASE OF SPERMATOZOA 142625 : HIRSUTISMSKELETAL DYSPLASIAMENTAL RETARDATION SYNDROME 142630 : HISTIOCYTOSIS, PROGRESSIVE MUCINOUS 142690 : HIDRADENITIS SUPPURATIVA, FAMILIAL 142700 : HIP, DISLOCATION OF, CONGENITAL 142730 : HISTIOCYTIC DERMATOARTHRITIS 142770 : HLA MODIFIER 142925 : MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, H PSEUDOGENE; HLAHP 142954 : HOMEO BOX 1E; HOX1E 142990 : HOMEO BOX X 143050 : HUMERORADIAL SYNOSTOSIS 143095 : HUMEROSPINAL DYSOSTOSIS 143150 : H-Y ANTIGEN RECEPTOR 143460 : 5-@HYDROXYTRYPTAMINE OXYGENASE REGULATOR; HTOR 143470 : HYPERALPHALIPOPROTEINEMIA 143860 : HYPERCHLORHIDROSIS, ISOLATED 143880 : HYPERCALCEMIA, IDIOPATHIC, OF INFANCY 144020 : HYPERCHOLESTEROLEMIA SUPPRESSOR 144050 : HYPERHEPARINEMIA 144100 : HYPERHIDROSIS, GUSTATORY 144110 : HYPERHIDROSIS PALMARIS ET PLANTARIS 144120 : HYPERIMMUNOGLOBULIN G1(A1) SYNDROME 144190 : HYPERKERATOSIS-HYPERPIGMENTATION SYNDROME 144300 : HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS 144600 : HYPERLIPOPROTEINEMIA, TYPE IV 144650 : HYPERLIPOPROTEINEMIA, TYPE V 144755 : HYPEROSTOSIS CRANIALIS INTERNA 144800 : HYPEROSTOSIS FRONTALIS INTERNA 145200 : HYPERPIGMENTATION OF FULDAUER AND KUIJPERS 145270 : HYPERPROGLUCAGONEMIA 145290 : HYPERREFLEXIA; HRX 145295 : HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL 145300 : HYPERSENSITIVITY PNEUMONITIS, FAMILIAL 145350 : HYPERTAURINURIC CARDIOMYOPATHY 145590 : HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA 146110 : HYPOGONADISM, ISOLATED HYPOGONADOTROPIC 146160 : HYPOMELIA WITH MULLERIAN DUCT ANOMALIES 146350 : HYPOPHOSPHATEMIC BONE DISEASE; HBD 146390 : HYPOPITUITARISM ASSOCIATED WITH 18p- SYNDROME 146400 : HYPOPLASIA OF TEETH ROOTS 146450 : HYPOSPADIAS 146500 : HYPOTENSION, ORTHOSTATIC 146580 : HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE SUPPRESSOR 146600 : ICHTHYOSIS HYSTRIX GRAVIOR 146692 : INOSINE MONOPHOSPHATE DEHYDROGENASE-LIKE 1; IMPDHL1 146720 : ICHTHYOSISCHEEKEYEBROW SYNDROME 146750 : ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT FORM 146830 : IMMUNE DEFICIENCY, FAMILIAL VARIABLE 146840 : IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST 146850 : IMMUNE SUPPRESSION; IS 146990 : IMMUNOGLOBULIN HEAVY CHAIN DIVERSITY REGION 2; IGHDY2 147060 : IMMUNOGLOBULIN E, ELEVATED, WITH NEUTROPHIL CHEMOTAXIS DEFECT, RECURRENT INFECTIONS, AND MUCOCUTANEOUS CANDIDIASIS 147250 : INCISORS, FUSED 147251 : INCISORS, FUSED MANDIBULAR 147260 : IMMUNOGLOBULIN SWITCH SEQUENCES 147300 : INCISORS, LONG UPPER CENTRAL 147320 : INSULIN RECEPTORS, FAMILIAL INCREASE IN 147330 : INCISORS, LOWER CENTRAL, ABSENCE OF 147350 : INCISORS, ROTATION OF UPPER CENTRAL 147400 : INCISORS, SHOVEL-SHAPED 147421 : INCLUSION BODY MYOSITIS 147430 : INDIFFERENCE TO PAIN 147530 : INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY 147540 : INSECT STINGS, HYPERSENSITIVITY TO 147560 : INTERFERON ANTIVIRAL DEPRESSOR 147590 : IRIS DYSPLASIA WITH OCULAR HYPERTELORISM, PSYCHOMOTOR RETARDATION AND SENSORINEURAL DEAFNESS 147610 : IRIS PIGMENT LAYER, CLEAVAGE OF 147630 : ISLET CELL ADENOMATOSIS 147710 : INTUSSUSCEPTION 147770 : JOHNSON NEUROECTODERMAL SYNDROME 147820 : INTERNAL CAROTID ARTERY, SPONTANEOUS DISSECTION OF 147920 : KABUKI SYNDROME 148000 : KAPOSI SARCOMA 148100 : KELOIDS 148210 : KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT 148300 : KERATOCONUS 148360 : KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORY NEUROPATHY 148390 : KERATOSES, FAMILIAL ACTINIC 148520 : KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY 148800 : KLEEBLATTSCHAEDEL SYNDROME 148840 : KLEINE-LEVIN HIBERNATION SYNDROME 148860 : KLIPPEL-FEIL DEFORMITY, CONDUCTIVE DEAFNESS, AND ABSENT VAGINA 148870 : KLIPPEL-FEIL DEFORMITY, DEAFNESS, AND FACIAL ASYMMETRY 149000 : KLIPPEL-TRENAUNAY-WEBER SYNDROME 149100 : KNUCKLE PADS 149500 : KYRLE DISEASE 149600 : LABIA MINORA, INCOMPLETE ADHESION OF 150160 : LACTATE DEHYDROGENASE-K; LDHK 150170 : LACTIC ACIDOSIS, CHRONIC ADULT FORM 150220 : LACTOSE INTOLERANCE, CONGENITAL 150280 : LARYNGOMALACIA 150300 : LARYNX, CONGENITAL PARTIAL ATRESIA OF 150360 : LARYNGEAL WEB, FAMILIAL 150500 : LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT 150550 : LAZY LEUKOCYTE SYNDROME 150590 : LEG ULCERS, FAMILIAL, OF JUVENILE ONSET 150600 : LEGG-CALVE-PERTHES DISEASE 150700 : LEIOMYOMA OF VULVA AND ESOPHAGUS 150900 : LENTIGINES 151000 : LENTIGINOSIS, CENTROFACIAL NEURODYSRAPHIC 151001 : LENTIGINOSIS, INHERITED PATTERNED 151050 : LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM 151380 : LEUKEMIA, ACUTE MONOCYTIC 151500 : LEUKOCYTE NUCLEAR APPENDAGES, HEREDITARY PREVALENCE OF 151550 : LEUKONYCHIA MACULATA 151590 : LICHEN SCLEROSUS ET ATROPHICUS; LSA 151610 : LEVATOR-MEDIAL RECTUS SYNKINESIS 151620 : LICHEN PLANUS, FAMILIAL 151640 : LIP, HAMARTOMATOUS 151680 : LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY, SHORT STATURE, AND INSULINOPENIC DIABETES MELLITUS 151700 : LIPOMA OF THE CONJUNCTIVA 151800 : LIPOMATOSIS, FAMILIAL BENIGN CERVICAL 152300 : LIPOPROTEIN TYPESLt SYSTEM 152400 : LIPOPROTEIN, VARIANT OF BETA 152420 : LITHIUM TRANSPORT 152423 : LIVER CELL ADHESION MOLECULE; LCAM 152430 : LONGEVITY 152450 : LOW DENSITY LIPOPROTEIN, VARIATION IN MOLECULAR WEIGHT 152550 : LUMBAR STENOSIS, FAMILIAL 152600 : LUNULAE OF FINGERNAILS 152900 : LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY 153000 : LYMPHEDEMA AND PTOSIS 153300 : LYMPHEDEMA, ADULT-ONSET, AND YELLOW NAILS 153360 : LYSOSOMAL GLYCOGEN STORAGE DISEASE WITH NORMAL ACID MALTASE ACTIVITY 153460 : MCARDLE SYNDROME 153470 : MACROCEPHALY, BENIGN FAMILIAL 153600 : MACROGLOBULINEMIA, WALDENSTROM; WM 153650 : MACROTHROMBOCYTOPATHY, NEPHRITIS, AND DEAFNESS 153670 : MACROTHROMBOCYTOPENIA, BENIGN MEDITERRANEAN 153870 : MACULAR DYSTROPHY, CONCENTRIC ANNULAR 153890 : MACULAR DYSTROPHY, FENESTRATED SHEEN TYPE 154000 : MACULES, HEREDITARY CONGENITAL HYPOPIGMENTED AND HYPERPIGMENTED 154300 : MALOCCLUSION DUE TO PROTUBERANT UPPER FRONT TEETH 154370 : MAMMASTATIN 154400 : ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1 154600 : MARCUS GUNN PHENOMENON 154750 : MARFANOID HYPERMOBILITY SYNDROME 154800 : MAST CELL DISEASE 154850 : MASTICATORY MUSCLES, HYPERTROPHY OF 155140 : MECKEL DIVERTICULUM 155145 : CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA 155150 : MEDIAN-ULNAR NERVE COMMUNICATIONS 155200 : MEDIOSTERNAL DEPIGMENTATION LINE 155500 : MEGALODACTYLY 155700 : MELANOMA, MALIGNANT INTRAOCULAR 155720 : MELANOMA, UVEAL 155755 : MELANOMA-ASTROCYTOMA SYNDROME 155770 : MELANOMA TUMOR ANTIGEN GP90 155950 : MELORHEOSTOSIS 156000 : MENIERE DISEASE 156190 : MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA 156200 : MENTAL RETARDATION, DOMINANT 156220 : MERALGIA PARAESTHETICA, FAMILIAL 156240 : MESOTHELIOMA, MALIGNANT 156250 : METACHONDROMATOSIS 156300 : METACHROMASIA OF FIBROBLASTS 156310 : METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASE A 156510 : METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY 156530 : METATROPIC DYSPLASIA, NONLETHAL DOMINANT 156620 : MICROCEPHALY-DEAFNESS SYNDROME 156700 : MICROCORNEA, GLAUCOMA AND ABSENT FRONTAL SINUSES 156830 : MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL 156900 : MICROPHTHALMOS WITH MYOPIA AND CORECTOPIA 157100 : MICROPHTHALMOS, PIGMENTARY RETINOPATHY, AND GLAUCOMA 157150 : MICROSPHEROPHAKIA WITH HERNIA 157151 : MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA 157160 : MICROTUBULE-ASSOCIATED PROTEIN TAU-LIKE; MAPTL 157300 : MIGRAINE 157500 : MILK PROTEINS, VARIANTS OF 157550 : MINICORE MYOPATHY, DOMINANT 157600 : MIRROR MOVEMENTS, HEREDITARY 157650 : MITOCHONDRIAL MYOPATHY, LIPID TYPE 157800 : MITRAL REGURGITATION, CONDUCTIVE DEAFNESS, AND FUSION OF CERVICAL VERTEBRAE AND OF CARPAL AND TARSAL BONES 157860 : MIXED LYMPHOCYTE CULTURE LOCUS II 157910 : MOEBIUS SYNDROME WITH CLUBFOOT, ARTHROGRYPOSIS, AND DIGITAL ANOMALIES 157960 : MOLONEY LEUKEMIA VIRUS INTEGRATION SITE 2, MOUSE, HOMOLOG OF; MLVI2 157980 : MOMO SYNDROME 158020 : MONOCLONAL ANTIBODY 4F2, ANTIGEN DEFINED BY, LIGHT CHAIN; M4F2L 158040 : MONOCLONAL ANTIBODY T87, CELL SURFACE GLYCOPROTEIN DEFINED BY; MSK2 158100 : MONOPHALANGY OF GREAT TOE 158250 : MOSAICISM, CHROMOSOMAL 158280 : MOTION SICKNESS 158330 : MULLERIAN APLASIA 158345 : MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS 158650 : MUSCULAR ATROPHY, MALIGNANT NEUROGENIC 158800 : MUSCULAR DYSTROPHY, BARNES TYPE 159100 : MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE 159300 : MUSICAL PERFECT PITCH 159400 : MYASTHENIA, FAMILIAL LIMB-GIRDLE 159410 : MYDRIATIC RESPONSE TO PHARMACOLOGIC AGENTS 159420 : MYDRIASIS, CONGENITAL 159500 : MYELINATED OPTIC NERVE FIBERS 159550 : MYELOCEREBELLAR DISORDER 159580 : MYELOPATHY, HTLV-1-ASSOCIATED; HAM 159700 : MYOCLONUS AND ATAXIA 159800 : MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS 159950 : MYOCLONUS, HEREDITARY, WITH PROGRESSIVE DISTAL MUSCULAR ATROPHY 160200 : MYOPATHY, CONGENITAL, WITH CRYSTALLINE INTRANUCLEAR INCLUSIONS 160550 : MYOPATHY, MITOCHONDRIAL, WITH CATARACT 160570 : MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS 160990 : MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS 161070 : NAIL HIGH-SULFUR PROTEIN 161080 : NAIL LOW-SULFUR PROTEIN 161100 : NAILBEDS, PIGMENTATION OF 161400 : NARCOLEPSY 161470 : NASAL ALAR COLLAPSE, BILATERAL 161480 : NASAL BONES, ABSENCE OF 161530 : NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE 161550 : NASOPHARYNGEAL CANCER 161600 : NAVICULAR BONE, ACCESSORY 161700 : NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF ADULT 161950 : NEPHRITIS, IgA TYPE 162020 : NERVE GROWTH FACTOR, ALPHA SUBUNIT; NGFA 162091 : SCHWANNOMATOSIS 162220 : NEUROFIBROMATOSIS, FAMILIAL INTESTINAL; NF3B 162240 : NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME 162260 : NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL; NF3A 162270 : NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI; NF4 162380 : NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE 162600 : NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE 162830 : NEUTROPHILIA, HEREDITARY 163050 : NEVUS ANEMICUS 163200 : NEVUS SEBACEUS OF JADASSOHN 163600 : NIPPLES INVERTED 163850 : NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES 163900 : NON-HEME PROTEIN OF ERYTHROCYTE 163955 : NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME 164000 : NOSE, ANOMALOUS SHAPE OF 164180 : OCULOCEREBROCUTANEOUS SYNDROME 164185 : OCULAR CICATRICIAL PEMPHIGOID; OCP 164190 : OCULAR DOMINANCE 164210 : OCULOAURICULOVERTEBRAL DYSPLASIA 164220 : OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS 164230 : OBSESSIVE-COMPULSIVE DISORDER 1; OCD1 164310 : OCULOPHARYNGODISTAL MYOPATHY 164330 : ODONTOMA-DYSPHAGIA SYNDROME 164600 : OLIVOPONTOCEREBELLAR ATROPHY IV 164680 : ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR 164745 : OMODYSPLASIA 164750 : OMPHALOCELE 164800 : ONYCHOLYSIS, PARTIAL, WITH SCLERONYCHIA 164891 : ONCOGENE YUASA 165098 : OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION 165150 : OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY 165199 : OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY 165200 : OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS 165300 : OPTIC ATROPHY, CATARACT, AND NEUROLOGIC DISORDER 165490 : OPTIC ATROPHY, DEAFNESS, OPHTHALMOPLEGIA, AND MYOPATHY 165510 : OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS 165550 : OPTIC NERVE HYPOPLASIA, FAMILIAL BILATERAL 165590 : ORAL-FACIAL-DIGITAL SYNDROME WITH FIBULAR APLASIA 165600 : ORBITAL MARGIN, HYPOPLASIA OF 165630 : ORGANOID NEVUS PHAKOMATOSIS 165660 : OSLAM SYNDROME 165670 : OSSIFIED EAR CARTILAGES 165680 : OSSICULAR MALFORMATIONS, FAMILIAL 165720 : OSTEOARTHROSIS, PRECOCIOUS; OAP 166000 : OSTEOCHONDROMATOSIS 166230 : OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES 166240 : OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH 166250 : OSTEOGLOPHONIC DWARFISM 166260 : OSTEOGENESIS IMPERFECTA WITH UNUSUAL SKELETAL LESIONS 166400 : OSTEOMAS OF MANDIBLE 166450 : OSTEOMESOPYKNOSIS 166705 : OSTEOPOIKILOSIS AND DACRYOCYSTITIS 166740 : OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES 166760 : OTITIS MEDIA, SUSCEPTIBILITY TO 166780 : OTOFACIOCERVICAL SYNDROME 166900 : OVALOCYTOSIS, HEREDITARY HEMOLYTIC 166910 : OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS 166950 : OVARIAN TERATOMA 166970 : OVARIAN FIBROMATA 166990 : OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA, HYDROCEPHALUS, AND HYPERTENSION 167100 : PACHYDERMOPERIOSTOSIS; PDP 167220 : PACMAN DYSPLASIA 167250 : PAGET DISEASE OF BONE 1; PDB1 167300 : PAGET DISEASE, EXTRAMAMMARY 167320 : PAGETOID AMYOTROPHIC LATERAL SCLEROSIS 167500 : PALATOPHARYNGEAL INCOMPETENCE 167600 : PALMARIS LONGUS MUSCLE, ABSENCE OF 167700 : PALMOMENTAL REFLEX 167750 : PANCREAS, ANNULAR 167755 : PANCREAS, DORSAL, AGENESIS OF 167850 : PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE 167870 : PANIC DISORDER 167900 : PAPILLOMATOSIS, FAMILIAL CUTANEOUS 167950 : PAPILLOMATOSIS, FLORID, OF NIPPLE 167959 : HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 1; HPV18I1 167960 : HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 2; HPV18I2 168100 : PARALYSIS AGITANS, JUVENILE, OF HUNT 168200 : PARAMOLAR TUBERCLE OF BOLK 168350 : PARAMYOTONIA WITHOUT COLD PARALYSIS 168400 : PARASTREMMATIC DWARFISM 168550 : PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA 168710 : PAROTID PROLINE-RICH SALIVARY PROTEIN Pc 168800 : PAROTIDOMEGALY, HEREDITARY BILATERAL 168830 : PASSOVOY FACTOR 168850 : PATELLA APLASIA, COXA VARA, AND TARSAL SYNOSTOSIS 168860 : PATELLA APLASIA OR HYPOPLASIA 168885 : PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA 169100 : PATENT DUCTUS ARTERIOSUS; PDA 169170 : PATTERSON PSEUDOLEPRECHAUNISM SYNDROME 169200 : PECHET FACTOR DEFICIENCY 169300 : PECTUS EXCAVATUM 169550 : PELVIS-SHOULDER DYSPLASIA 169610 : PEMPHIGUS VULGARIS, FAMILIAL 170600 : PERIODIC PARALYSIS III 170700 : PERIPHERAL DYSOSTOSIS 170900 : PERNICIOUS ANEMIA 170950 : PERNIOSIS 170980 : PERONEAL NERVE, ACCESSORY DEEP 170990 : PEROXIDASE, SALIVARY; SAPX 171100 : PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN 171350 : PHEOCHROMOCYTOMA, FAMILIAL EXTRAADRENAL 171420 : PHEOCHROMOCYTOMAISLET CELL TUMOR SYNDROME 171450 : PHLEBECTASIA OF LIPS 171480 : PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA 171660 : PHOSPHATASE, ACID, OF TISSUES 171700 : ALKALINE PHOSPHATASE, BLOOD GROUP-ASSOCIATED 171850 : PHOSPHOFRUCTOKINASE, RED CELL 172110 : PHOSPHOGLUCOMUTASE 4 172290 : PHOSPHOGLYCOPROTEIN 1; PGP1 172300 : PHOSPHOHEXOKINASE 172500 : PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION 172850 : PIEBALD TRAIT WITH NEUROLOGIC DEFECTS 172870 : PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY; PPCRA 172880 : PIERRE ROBIN SYNDROME AND OLIGODACTYLY 173000 : PILONIDAL SINUS 173340 : PLASMINOGEN-LIKE; PLGL 173395 : PLATELET ADENYLATE CYCLASE ACTIVITY 173400 : PLATELET AGGREGATION, SPONTANEOUS 173420 : PLATELET DISORDER, UNDEFINED 173450 : PLATELET FACTOR 3 DEFICIENCY 173560 : PLATELET MEMBRANE FLUIDITY; PMF 173580 : PLATELET RESPONSIVENESS TO ADRENALINE, DEPRESSED 173590 : PLATELET SIGNAL PROCESSING DEFECT 173700 : POIKILODERMA, HEREDITARY SCLEROSING 173750 : POLAND-MOEBIUS SYNDROME 173800 : POLAND SYNDROME 174100 : POLYDACTYLY, IMPERFORATE ANUS, AND VERTEBRAL ANOMALIES 174300 : POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP 174310 : POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA 174400 : POLYDACTYLY, PREAXIAL I 174770 : POLYMORPHIC LIGHT ERUPTION, HEREDITARY; HPLE 175050 : POLYPOSIS, GENERALIZED JUVENILE, WITH PULMONARY ARTERIOVENOUS MALFORMATION 175400 : POLYPOSIS, INTESTINAL, SCATTERED AND DISCRETE 175450 : POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES 175500 : POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES 175505 : POLYPOSIS OF GASTRIC FUNDUS WITHOUT POLYPOSIS COLI 175510 : POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL 175750 : POPLITEAL CYST 175850 : POROKERATOSIS PLANTARIS, PALMARIS ET DISSEMINATA 176090 : PORPHYRIA CUTANEA TARDA, TYPE I 176240 : POSTAXIAL OLIGODACTYLY, TETRAMELIC 176250 : POSTERIOR COLUMN ATAXIA 176305 : PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS 176440 : PREMATURE OVARIAN FAILURE AND BLEPHAROPHIMOSIS 176600 : PRESENILE DEMENTIA, KRAEPELIN TYPE 176620 : PRIAPISM, FAMILIAL IDIOPATHIC 176630 : PRIMARY RELEASE DISORDER OF PLATELETS 176670 : PROGERIA 176690 : PROGEROID SHORT STATURE WITH PIGMENTED NEVI 176780 : PROLAPSE OF VAGINA AND RECTUM 176800 : PRONATION-SUPINATION OF THE FOREARM, IMPAIRMENT OF 176900 : PROTEOLYTIC CAPACITY OF PLASMA 176920 : PROTEUS SYNDROME 177100 : PRURITUS, HEREDITARY LOCALIZED 177150 : PSEUDOACHONDROPLASTIC DYSPLASIA I 177300 : PSEUDOARTHROGRYPOSIS 177350 : PSEUDOATROPHODERMA COLLI 177600 : PSEUDOCHOLINESTERASE, INCREASE IN PLASMA LEVEL OF 177650 : PSEUDOEXFOLIATION OF THE LENS 177700 : PSEUDOGLAUCOMA 177800 : PSEUDOPAPILLEDEMA 177860 : PSEUDOXANTHOMA ELASTICUM, DOMINANT TYPE II 177980 : PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES 177990 : PTERYGIUM COLLI, ISOLATED 178000 : PTERYGIUM OF CONJUNCTIVA AND CORNEA 178110 : PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT TYPE 178330 : PTOSIS, STRABISMUS, AND ECTOPIC PUPILS 178370 : PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT 178400 : PULMONARY EDEMA OF MOUNTAINEERS 178500 : PULMONARY FIBROSIS, IDIOPATHIC 178550 : PULMONARY HEMOSIDEROSIS 178610 : PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL 178650 : PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHIC ABNORMALITIES 178651 : PULMONIC STENOSIS AND DEAFNESS 178800 : PUPIL, EGG-SHAPED 178900 : PUPILLARY MEMBRANE, PERSISTENCE OF 178995 : PRURITIC URTICARIAL PAPULES AND PLAQUES OF PREGNANCY; PUPPP 179000 : PURPURA SIMPLEX 179010 : PYLORIC STENOSIS, INFANTILE 179040 : PYRUVATE KINASE 2; PK2 179250 : RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARY DIASTEMA 179270 : RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA 179280 : RADIAL-RENAL SYNDROME 179300 : RADIOULNAR SYNOSTOSIS 179400 : RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE 179450 : RAGWEED SENSITIVITY 179500 : RAINDROP HYPOPIGMENTATION 179760 : RENAL CELL CARCINOMA 2; RCC2 179770 : RENAL CELL CARCINOMA 3; RCC3 179830 : RENAL TUBULAR ACIDOSIS, FAMILIAL PROXIMAL 179840 : RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM 179850 : RETICULAR PIGMENTED ANOMALY OF FLEXURES 180040 : RETINAL DEGENERATION 3; RD3 180060 : RETINAL FOLDS WITH MICROCEPHALY AND MICROPHTHALMOS 180070 : RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT 180080 : RETINAL VENOUS BEADING 180102 : RETINITIS PIGMENTOSA 5; RP5 180210 : RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT 180270 : RETINOSCHISIS, AUTOSOMAL DOMINANT 180300 : RHEUMATOID ARTHRITIS 180330 : RHEUMATOID FACTOR IgM IDIOTYPES 180350 : RHEUMATOID NODULOSIS 180360 : RHINY 180550 : RING DERMOID OF CORNEA 180730 : ROMBO SYNDROME 180750 : ROBINOW-SORAUF SYNDROME 180850 : RUBINSTEIN-LIKE SYNDROME 180870 : RUVALCABA SYNDROME 180930 : SALIVARY PROTEIN I; SAL-I 180940 : SALIVARY PROTEIN II; SAL-II 181000 : SARCOIDOSIS 181010 : SALIVARY DUCT CALCULI 181180 : SAY SYNDROME 181200 : SC(1) TRAIT OF SALIVA 181250 : SCALP DEFECTS AND POSTAXIAL POLYDACTYLY 181270 : SCALP-EAR-NIPPLE SYNDROME 181300 : SCAPULA, CONTOUR OF VERTEBRAL BORDER OF 181510 : SCHIZOPHRENIA 1; SCZD1 181700 : SCLEROCORNEA 181800 : SCOLIOSIS, IDIOPATHIC 182000 : SEBORRHEIC KERATOSES 182150 : SIMOSA CRANIOFACIAL SYNDROME 182170 : SIDEROBLASTIC ANEMIA WITH ERYTHROCYTE DIMORPHISM 182190 : SINUS NODE DISEASE AND MYOPIA 182200 : SELLA TURCICA, BRIDGED 182210 : SHPRINTZEN OMPHALOCELE SYNDROME 182220 : SISTER CHROMATID EXCHANGE, FREQUENCY OF 182255 : SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION 182260 : SLIPPED FEMORAL CAPITAL EPIPHYSES 182269 : SMALL PROLINE-RICH PROTEIN 2C; SPRR2C 182270 : SMELL KETONE COMPOUNDS, ABILITY TO 182370 : SODIUM-POTASSIUM-ATPase, BETA-POLYPEPTIDE-LIKE 182400 : SOMATOMEDIN, EMBRYONIC 182410 : SNEDDON SYNDROME 182610 : SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPERM 182690 : SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND PROGRESSIVE NEPHROPATHY 182700 : SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS 182800 : SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS 182815 : SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA 182820 : SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY 182830 : SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA 182875 : SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, AND TRANSVERSE EARLOBE CREASE 182882 : SPERM PROTAMINE P4; PRM4 182930 : SPHINCTER OF ODDI, FAMILIAL HYPERTROPHY OF 182940 : SPINA BIFIDA 182960 : SPINAL MUSCULAR ATROPHY, DISTAL 182990 : SPINAL INTRADURAL ARACHNOID CYSTS 183020 : SPINAL MUSCULAR ATROPHY, SEGMENTAL 183100 : SPINOCEREBELLAR ATROPHY WITH PUPILLARY PARALYSIS 183250 : SPLENIN 183300 : SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA 183400 : SPLIT LOWER LIP 183500 : SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA 183700 : SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS 183800 : SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS 183802 : SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATIC DEFECTS 183840 : SPONDYLOARTHROPATHY, AUTOSOMAL DOMINANT 183849 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS 183850 : SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY 184000 : SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS 184095 : SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE 184200 : SPONDYLOLISTHESIS 184253 : SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE 184260 : SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA 184300 : SPONDYLOSIS, CERVICAL 184450 : STAMMERING 184460 : STAPES ANKYLOSIS WITH BROAD THUMB AND TOES 184510 : STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH 184705 : STEINFELD SYNDROME 184800 : STERNUM, PREMATURE OBLITERATION OF SUTURES OF 184850 : STIFF MAN SYNDROME, HEREDITARY FORM OF 185020 : STOMATOCYTOSIS, COLD-SENSITIVE 185069 : STORM SYNDROME 185070 : STORMORKEN SYNDROME 185100 : STRABISMUS 185120 : STRATTON-PARKER SYNDROME 185300 : STURGE-WEBER SYNDROME 185400 : SUBGLOTTIC BAR 185450 : SUBLUXATION OF LENSES, LATE 185460 : SULFHEMOGLOBINEMIA, CONGENITAL 185480 : SUPRABULBAR PARESIS, CONGENITAL 185540 : SURFACE ANTIGEN, GLYCOPROTEIN 75 185595 : SURFACE ANTIGEN OF ACTIVATED B CELLS, BB1; BB1 185600 : SYMPHALANGISM OF TOES 185610 : SURFACE POLYPEPTIDES, ANONYMOUS 185642 : SURFEIT 6; SURF6 185650 : SYMPHALANGISM, C. S. LEWIS TYPE 185750 : SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET 186200 : SYNDACTYLY, TYPE IV 186575 : SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM 186600 : SYRINGOMAS, MULTIPLE 186700 : SYRINGOMYELIA 186750 : TALONAVICULAR COALITION 186920 : T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA ANTIGEN; TALLA 186950 : T-CELL SUBGROUPS, NON-HLA-LINKED 187030 : T-COMPLEX LOCUS TCP10B; TCP10B 187050 : TEETH PRESENT AT BIRTH 187100 : TEETH, SUPERNUMERARY 187340 : TEMPERATURE-SENSITIVE LETHAL MUTATION 187350 : TELECANTHUS 187360 : TEMPORAL ARTERITIS 187390 : TENDONS, EXTENSOR, OF FINGERS, ANOMALOUS INSERTION OF 187400 : TESTICULAR TORSION 187500 : TETRALOGY OF FALLOT 187501 : TETRALOGY OF FALLOT AND GLAUCOMA 187510 : TETRAMELIC MONODACTYLY 187550 : THALASSEMIA, BETA+, SILENT ALLELE 187750 : THORACIC DYSOSTOSIS, ISOLATED 187760 : THORACOLARYNGOPELVIC DYSPLASIA; TLPD 187770 : THORACOPELVIC DYSOSTOSIS 187800 : GLANZMANN THROMBASTHENIA; GTA 187940 : THROMBOCYTE B; THB 188020 : THROMBOCYTOPENIA, CYCLIC 188025 : THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT 188030 : THROMBOCYTOPENIC PURPURA, AUTOIMMUNE 188035 : THROMBOGLOBULIN, BETA-2; TGB2 188100 : THUMB DEFORMITY 188150 : THUMB DEFORMITY AND ALOPECIA 188200 : THUMBNAILS, ABSENT 188201 : THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY 188455 : THYROGLOSSAL DUCT CYST, FAMILIAL 188470 : THYROID CARCINOMA, FOLLICULAR; FTC 188560 : THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT 188580 : THYROTOXIC PERIODIC PARALYSIS 188600 : THYROXINE-BINDING GLOBULIN OF SERUM 188700 : TIBIA VARA 188740 : TIBIA, ABSENCE OF, WITH POLYDACTYLY 189000 : TOE, FIFTH, NUMBER OF PHALANGES IN 189100 : TOE, MISSHAPEN 189150 : TOE, ROTATED FIFTH 189200 : TOES, RELATIVE LENGTH OF FIRST AND SECOND 189230 : TOES, SPACE BETWEEN FIRST AND SECOND 189300 : TONGUE CURLING, FOLDING, OR ROLLING 189490 : TOOTH MALFORMATION 189600 : TORTICOLLIS 189800 : PREECLAMPSIA/ECLAMPSIA 1; PEE1 189960 : TRACHEOESOPHAGEAL FISTULA WITH OR WITHOUT ESOPHAGEAL ATRESIA 189961 : TRACHEOPATHIA OSTEOPLASTICA 189974 : TRANSDUCIN, BETA POLYPEPTIDE 190200 : TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS 190330 : TRICHOMEGALY 190340 : TRICHODISCOMAS, FAMILIAL MULTIPLE 190345 : TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC 190360 : TRICHODYSPLASIA-XERODERMA 190400 : TRIGEMINAL NEURALGIA 190410 : TRIGGER THUMB 190420 : TRIGLYCERIDE STORAGE DISEASE, TYPE I 190430 : TRIGLYCERIDE STORAGE DISEASE, TYPE II 190440 : TRIGONOCEPHALY 190445 : TRIIODOTHYRONINE RECEPTOR AUXILIARY PROTEIN; TRAP 190500 : TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES 190650 : TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA 190800 : TRISTICHIASIS 191000 : TROCHLEA OF THE HUMERUS, APLASIA OF 191090 : TUBEROUS SCLEROSIS 4; TSC4 191091 : TUBEROUS SCLEROSIS 3; TSC3 191150 : TUFTSIN DEFICIENCY 191250 : TWINNING DUE TO SUPERFETATION 191270 : TYROSINASE-LIKE; TYRL 191400 : ULNA AND FIBULA, HYPOPLASIA OF 191420 : ULNA METAPHYSEAL DYSPLASIA SYNDROME 191440 : ULNAR HYPOPLASIA 191482 : UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, AND BRACHYDACTYLY 191600 : URETER, CANCER OF 191650 : URETEROCELE 191700 : URIC ACID UROLITHIASIS 191800 : URINARY BLADDER, ATONY OF 191850 : URTICARIA, AQUAGENIC 191950 : URTICARIA, FAMILIAL LOCALIZED HEAT 192000 : UTERINE ANOMALIES 192050 : UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS 192100 : UVULA, BIFID 192200 : VARICOSE VEINS 192300 : VASCULAR HELIX OF UMBILICAL CORD 192310 : VASCULITIS, HEREDITARY INFLAMMATORY, WITH PERSISTENT NODULES 192350 : VATER ASSOCIATION 192400 : VEINS, PATTERN OF, ON ANTERIOR THORAX 192445 : VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE 192450 : VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL 192700 : VENULAR INSUFFICIENCY, SYSTEMIC 192800 : VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS 192950 : VERTICAL TALUS, CONGENITAL; CVT 193000 : VESICOURETERAL REFLUX; VUR 193003 : VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS 193005 : VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE 193007 : VESTIBULOPATHY, FAMILIAL 193050 : VIBRATORY ANGIOEDEMA 193070 : VIRUS RD114 RNA COMPLEMENTARITY 193200 : VITILIGO 193230 : VITREORETINAL DEGENERATION, SNOWFLAKE TYPE 193240 : VOCAL CORD PARALYSIS AND PTOSIS 193450 : VULVOVAGINITIS, ALLERGIC SEMINAL 193670 : WHIM SYNDROME 193675 : 'WHIRLER' DEAFNESS, HUMAN HOMOLOG OF; WI 193680 : WHISPERING DYSPHONIA, HEREDITARY 194000 : WIDOW'S PEAK 194100 : WISDOM TEETH, ABSENCE OF 194200 : WOLFF-PARKINSON-WHITE SYNDROME 194320 : WORONETS TRAIT 194370 : X-RAY SENSITIVITY; XRS 194400 : XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD 194522 : ZINC FINGER PROTEIN 11B; ZNF11B | |
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