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DEVELOPMENT OF NEURAL CREST |
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Introduction
Below are entries from a search of the Online Mendelian Inheritance in Man database. With Internet connection, clicking on the entry number will show the complete entry.
74 entries found, searching for
"neural crest"
*602407 HEART- AND NEURAL CREST DERIVATIVES-EXPRESSED 2; HAND2
*602150 SLUG, CHICKEN, HOMOLOG OF; SLUG
*602406 HEART- AND NEURAL CREST DERIVATIVES-EXPRESSED 1; HAND1
*602229 SRY-BOX 10; SOX10
*193500 WAARDENBURG SYNDROME, TYPE I; WS1
*131240 ENDOTHELIN 1; EDN1
*162200 NEUROFIBROMATOSIS, TYPE I; NF1
*188400 DIGEORGE SYNDROME; DGS
#171400 MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2
*162660 NEUROTROPHIN 3; NTF3
*131244 ENDOTHELIN RECEPTOR, TYPE B; EDNRB
#277580 WAARDENBURG-SHAH SYNDROME
*604240 HOMEO BOX 11-LIKE 1; HOX11L1
*131242 ENDOTHELIN 3; EDN3
600501 ABCD SYNDROME
*600423 ENDOTHELIN-CONVERTING ENZYME 1; ECE1
*600237 HISTONE CELL CYCLE REGULATION DEFECTIVE, S. CEREVISIAE, HOMOLOG OF, A; HIRA
*256700 NEUROBLASTOMA
#142623 HIRSCHSPRUNG DISEASE
#162300 MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B
#130650 BECKWITH-WIEDEMANN SYNDROME; BWS
164210 OCULOAURICULOVERTEBRAL DYSPLASIA
*164761 RET PROTOONCOGENE; RET
*123101 MSH (DROSOPHILA) HOMEO BOX HOMOLOG 2; MSX2
*106210 PAIRED BOX GENE 6; PAX6
#171300 PHEOCHROMOCYTOMA
604651 GROWTH/DIFFERENTIATION FACTOR 7; GDF7
*601280 MAB21, C. ELEGANS, HOMOLOG-LIKE 1; MAB21L1
#176270 PRADER-WILLI SYNDROME; PWS
#256800 INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA
*300109 PROTEIN PHOSPHATASE, EF-HAND CALCIUM-BINDING DOMAIN 1; PPEF1
*603851 PAIRED MESODERM HOMEO BOX 2B; PMX2B
#193510 WAARDENBURG SYNDROME, TYPE IIA; WS2A
#209880 AUTONOMIC CONTROL, CONGENITAL FAILURE OF
214800 CHOANAL ATRESIA, POSTERIOR; PCA
*600594 DIGEORGE CRITICAL REGION GENE 2
*604357 MAB21, C. ELEGANS, HOMOLOG-LIKE 2; MAB21L2
600459 ARTERIAL DISSECTION WITH LENTIGINOSIS
*601754 UBIQUITIN FUSION DEGRADATION 1-LIKE; UFD1L
249400 MELANOSIS, NEUROCUTANEOUS
*155735 MELANOMA ADHESION MOLECULE; MCAM
*167415 PAIRED BOX GENE 8; PAX8
*153245 LYMPHOID ENHANCER-BINDING FACTOR 1; LEF1
217100 CONSTRICTING BANDS, CONGENITAL
*151442 LEUKEMIA-ASSOCIATED PHOSPHOPROTEIN p18; LAP18
*600408 DISCOIDIN DOMAIN RECEPTOR FAMILY, MEMBER 1; DDR1
#146150 HYPOMELANOSIS OF ITO; HMI
#137600 IRIDOGONIODYSGENESIS, TYPE 2; IRID2
*164920 V-KIT HARDY-ZUCKERMAN 4 FELINE SARCOMA VIRAL ONCOGENE HOMOLOG; KIT
#188550 THYROID CARCINOMA, PAPILLARY
*305424 FACTOR VIII-ASSOCIATED GENE 2
*601499 RIEGER SYNDROME, TYPE 2; RIEG2
*601601 TRANSCRIPTION FACTOR AP2-BETA; TFAP2B
*601602 TRANSCRIPTION FACTOR AP2-GAMMA; TFAP2C
#601631 IRIDOGONIODYSGENESIS, TYPE 1; IRID1
*601654 EYES ABSENT 2; EYA2
*600525 DISTAL-LESS HOMEO BOX 3; DLX3
*601845 GOOSECOID-LIKE; GSCL
*126255 DISTAL-LESS HOMEO BOX 2; DLX2
*121014 GAP JUNCTION PROTEIN, ALPHA-1; GJA1
#118200 CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B; CMT1B
#106200 ANIRIDIA; AN1
*602942 NEUROBLASTOMA STAGE 4S GENE
*603054 GREMLIN
*603129 LIM DOMAIN ONLY 4; LMO4
603260 BARH-LIKE HOMEO BOX-1
603288 KERATOCAN; KERA
603807 PETERS ANOMALY WITH CATARACT
*601090 FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 7; FKHL7
*603886 ARTEMIN; ARTN
About Notes
- Notes from the Embryology Program compiled and written by Dr Mark Hill.
- Note Links to OMIM Entries and PubMed are copies of originals for computers without internet access. Computers with internet access can directly access these databases.
- Note that reference lists are only relevant to the date that the original search was carried out.
m.hill@unsw.edu.au
Date Last Modified: 22/7/99
This site maintained by Dr M. Hill