All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01113 MCCRP1 microcephaly and chorioretinopathy, autosomal recessive, type 1 (MCCRP-1) 251270 AR 1 2 TUBGCP6 - -
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