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All: 186 
OMIM dbSNP: 7 
OMIM UniSTS: 37 
Items 1 - 20 of 186
 
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1: 302380 Links
CATEL-MANZKE SYNDROME
2: %112700 Links
BRACHYDACTYLY, TYPE A3; BDA3
3: 148520 Links
KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY
4: %609625 Links
CHROMOSOME 10q DELETION SYNDROME
Gene map locus 10q
5: %180860 GeneTests, Links
SILVER-RUSSELL SYNDROME; SRS
Gene map locus 11p15.5, 7p11.2
6: #140000 GeneTests, Links
HAND-FOOT-UTERUS SYNDROME
Gene map locus 7p15-p14.2
7: #149730 GeneTests, Links
LACRIMOAURICULODENTODIGITAL SYNDROME; LADD
Gene map locus 5p13-p12, 4p16.3
8: %261540 GeneTests, Links
PETERS-PLUS SYNDROME
9: %227330 Links
FACIODIGITOGENITAL SYNDROME, RECESSIVE
10: #169100 GeneTests, Links
CHAR SYNDROME
Gene map locus 6p12
11: #122470 GeneTests, Links
CORNELIA DE LANGE SYNDROME; CDLS
Gene map locus 5p13.1
12: #170390 GeneTests, Links
ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS
Gene map locus 17q23.1-q24.2
13: #187500 Links
TETRALOGY OF FALLOT
Gene map locus 20p12, 8q23, 5q34
14: %157950 Links
MOLAR I REINCLUSION
15: %609432 Links
SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION; MSSD
16: #608093 Links
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij
Gene map locus 11q23.3
17: 607552 Links
MINICORE MYOPATHY, ANTENATAL ONSET, WITH ARTHROGRYPOSIS
18: 602249 Links
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES
19: %600990 Links
LAGOPHTHALMIA WITH BILATERAL CLEFT LIP AND PALATE
20: 600123 Links
ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS
Items 1 - 20 of 186
 
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Jun 21 2006 12:14:26