All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05153 MCPH microcephaly, primary, autosomal recessive (MCPH) - - 8 8 CEP152, MCPH1, MFSD2A, WDFY3 - -
04576 NEDMISBA;MCPH15 neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalitie (MCPH15) 616486 AR 11 11 MFSD2A - -
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