UNSW Embryology
DEVELOPMENT OF THE GASTROINTESTINAL SYSTEM
Select Entries from OMIM |
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This page is for computers without external internet access. Normally the blue numbers below would link to a full description of the abnormality. |
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50 entries found, searching for
"hirschsprung" #142623 HIRSCHSPRUNG DISEASE #277580 WAARDENBURG-SHAH SYNDROME #209880 AUTONOMIC CONTROL, CONGENITAL FAILURE OF *600156 HIRSCHSPRUNG DISEASE 3 #600155 HIRSCHSPRUNG DISEASE 2; HSCR2 235730 HIRSCHSPRUNG DISEASE, MICROCEPHALY, AND IRIS COLOBOMA 235760 HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIAL FEATURES 235740 HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS 306980 HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY 235750 HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIG TOES, AND VENTRICULAR SEPTAL DEFECT 235735 HIRSCHSPRUNG DISEASE WITH BILATERAL BICOLORED IRIDES *164761 RET PROTOONCOGENE; RET *131244 ENDOTHELIN RECEPTOR, TYPE B; EDNRB *131242 ENDOTHELIN 3; EDN3 *600837 GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; GDNF *602229 SRY-BOX 10; SOX10 *193500 WAARDENBURG SYNDROME, TYPE I; WS1 #193510 WAARDENBURG SYNDROME, TYPE IIA; WS2A *602018 NEURTURIN; NRTN *600423 ENDOTHELIN-CONVERTING ENZYME 1; ECE1 *308840 L1 CELL ADHESION MOLECULE; L1CAM *600065 INTEGRIN, BETA-2; ITGB2 #155240 MEDULLARY THYROID CARCINOMA, FAMILIAL; MTC1 *300048 INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED #172800 PIEBALD TRAIT; PBT *209900 BARDET-BIEDL SYNDROME, TYPE 2; BBS2 #115470 CAT EYE SYNDROME; CES *250250 CARTILAGE-HAIR HYPOPLASIA; CHH #190685 TRISOMY 21 *255320 MYOPATHY, CONGENITAL MULTICORE, WITH EXTERNAL OPHTHALMOPLEGIA *259700 OSTEOPETROSIS, AUTOSOMAL RECESSIVE *221350 DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA *236700 MCKUSICK-KAUFMAN SYNDROME; MKKS #268670 RUTLEDGE LETHAL MULTIPLE CONGENITAL ANOMALY SYNDROME #270400 SMITH-LEMLI-OPITZ SYNDROME, TYPE I *304100 CORPUS CALLOSUM, PARTIAL AGENESIS OF *601496 GDNF FAMILY RECEPTOR ALPHA-1; GFRA1 208530 ASPLENIA WITH CARDIOVASCULAR ANOMALIES 202550 AGANGLIONOSIS, TOTAL INTESTINAL #171400 MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2 #171300 PHEOCHROMOCYTOMA #162300 NEUROMATA, MUCOSAL, WITH ENDOCRINE TUMORS *156845 MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF 154400 ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1 601223 NEURONAL INTESTINAL DYSPLASIA, TYPE B; NID B 223200 DISORGANIZATION, MOUSE, HOMOLOG OF ^601669 MOVED TO 602229 #148820 KLEIN-WAARDENBURG SYNDROME *126800 DUANE SYNDROME *602523 DOWN SYNDROME CELL ADHESION MOLECULE; DSCAM |
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