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All: 42 
OMIM dbSNP: 1 
OMIM UniSTS: 5 
Items 1 - 20 of 42
 
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1: #192430 GeneTests, Links
VELOCARDIOFACIAL SYNDROME
Gene map locus 22q11.2
2: 103300 Links
AGLOSSIA-ADACTYLIA
HANHART SYNDROME, INCLUDED
3: #606056 GeneTests, Links
GLUCOSIDASE I DEFICIENCY
Gene map locus 2p13-p12
4: #300472 Links
CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA, AND MICROGNATHIA
Gene map locus Xq13.1-q13.3
5: #277590 Links
WEAVER SYNDROME
WEAVER-LIKE SYNDROME, INCLUDED
Gene map locus 5q35
6: #261515 GeneTests, Links
D-BIFUNCTIONAL PROTEIN DEFICIENCY
Gene map locus 5q2, 3p23-p22
7: 245552 Links
LAMBOTTE SYNDROME
8: %235510 Links
HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME
9: 165590 Links
OROFACIODIGITAL SYNDROME X; OFD10
10: #609192 GeneTests, Links
LOEYS-DIETZ SYNDROME; LDS
Gene map locus 9q33-q34, 3p22
11: 600331 Links
PARC SYNDROME
12: %309610 Links
PRIETO X-LINKED MENTAL RETARDATION SYNDROME; PRS
Gene map locus Xp11-q21
13: 300280 Links
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
14: %270750 Links
SPASTIC PARAPLEGIA 23; SPG23
15: 227270 Links
FACIOCARDIOMELIC DYSPLASIA, LETHAL
16: %206920 Links
ANOPHTHALMOS WITH LIMB ANOMALIES
17: %194350 Links
WT LIMB-BLOOD SYNDROME
18: #154700 GeneTests, Links
MARFAN SYNDROME; MFS
Gene map locus 15q21.1
19: #141750 Links
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, DELETION-TYPE
Gene map locus 16pter-p13.3
20: 225040 Links
ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESIS OF THE CORPUS CALLOSUM
Items 1 - 20 of 42
 
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Jun 21 2006 12:14:26