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
05060 COXPD20 oxidative phosphorylation deficiency, combined, type 20 (COXPD-20) 615917 AR - - VARS2 - -
05376 NDMSCA neurodevelopmental disorder with microcephaly, seizures, cortical atrophy (NDMSCA) 617802 AR 1 1 VARS - autosomal recessive
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