All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05053 MCCRP3 microcephaly and chorioretinopathy, autosomal recessive, type 3 (MCCRP-3) 616335 - - - TUBGCP4 - -
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