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Sequencing Progress
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All: 111 
OMIM dbSNP: 6 
OMIM UniSTS: 24 
Items 1 - 20 of 111
 
 of 6
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1: %143400 Links
MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MRD
Gene map locus 6p
2: %236730 Links
UROFACIAL SYNDROME; UFS
Gene map locus 10q23-q24
3: 604916 Links
HYDRONEPHROSIS, CONGENITAL, WITH CLEFT PALATE, CHARACTERISTIC FACIES, HYPOTONIA, AND MENTAL RETARDATION
4: 605311 Links
ARTHROGRYPOSIS, DISTAL, WITH PECULIAR FACIES AND HYDRONEPHROSIS
5: %269150 Links
SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME
6: 183802 Links
SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATIC DEFECTS
7: %606170 Links
GENITOPATELLAR SYNDROME
8: %249210 Links
MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME
Gene map locus 15q24
9: 192350 GeneTests, Links
VATER ASSOCIATION
VACTERL ASSOCIATION, INCLUDED
10: 163850 Links
NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES
11: 104350 Links
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM
12: 602418 Links
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME
13: #142945 GeneTests, Links
HOLOPROSENCEPHALY 3; HPE3
Gene map locus 7q36
14: %607598 Links
LETHAL CONGENITAL CONTRACTURE SYNDROME 2
15: %600383 Links
MESOMELIA-SYNOSTOSES SYNDROME
16: *314390 Links
VACTERL ASSOCIATION WITH HYDROCEPHALUS, X-LINKED
17: %305600 Links
FOCAL DERMAL HYPOPLASIA; DHOF
18: #304150 GeneTests, Links
CUTIS LAXA, X-LINKED
Gene map locus Xq12-q13
19: #304120 GeneTests, Links
OTOPALATODIGITAL SYNDROME, TYPE II; OPD2
Gene map locus Xq28, Xq28
20: #301040 GeneTests, Links
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED; ATRX
Gene map locus Xq13
Items 1 - 20 of 111
 
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Jun 21 2006 12:14:26