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All: 451 
OMIM dbSNP: 30 
OMIM UniSTS: 105 
Items 1 - 20 of 451
 
 of 23
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1: #251260 GeneTests, Links
NIJMEGEN BREAKAGE SYNDROME
BERLIN BREAKAGE SYNDROME, INCLUDED; BBS, INCLUDED
Gene map locus 8q21
2: %152950 GeneTests, Links
LYMPHEDEMA, MICROCEPHALY, CHORIORETINOPATHY SYNDROME
3: #164280 GeneTests, Links
FEINGOLD SYNDROME
Gene map locus 2p24.1
4: %251270 Links
MICROCEPHALY WITH CHORIORETINOPATHY, AUTOSOMAL RECESSIVE
5: %251290 Links
PSEUDO-TORCH SYNDROME
6: 156590 Links
MICROCEPHALY WITH CHORIORETINOPATHY, AUTOSOMAL DOMINANT
7: %251300 Links
MICROCEPHALY, HIATUS HERNIA, AND NEPHROTIC SYNDROME
8: 212540 Links
CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME
CATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED
9: 243605 Links
JEJUNAL ATRESIA WITH MICROCEPHALY AND OCULAR ANOMALIES
10: #607196 GeneTests, Links
MICROCEPHALY, AMISH TYPE; MCPHA
Gene map locus 17q25.3
11: 203340 Links
ALBINISM-MICROCEPHALY-DIGITAL ANOMALIES SYNDROME
12: #251200 Links
MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1; MCPH1
Gene map locus 19q13.1-q13.2, 15q15-q21, 8p23
13: *605481 Links
ABNORMAL SPINDLE-LIKE, MICROCEPHALY-ASSOCIATED; ASPM
Gene map locus 1q31
14: #608716 Links
MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 5; MCPH5
Gene map locus 1q31
15: %156580 Links
MICROCEPHALY, AUTOSOMAL DOMINANT
16: %272440 Links
SYNDACTYLY, TYPE I, WITH MICROCEPHALY AND MENTAL RETARDATION
17: #606858 Links
PREMATURE CHROMOSOME CONDENSATION WITH MICROCEPHALY AND MENTAL RETARDATION
Gene map locus 8p23
18: 251280 Links
MICROCEPHALY WITH SPASTIC QUADRIPLEGIA
19: %608027 Links
CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY
Gene map locus 7q11-q21
20: #235730 GeneTests, Links
MOWAT-WILSON SYNDROME
Gene map locus 2q22
Items 1 - 20 of 451
 
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