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
04592 LSDMCA3 skin defects, linear, with multiple congenital anomalies, type 3 (LSDMCA-3) 300952 XLD - - NDUFB11 - -
06861 MC1DN30 ?Mi complex I deficiency, nuclear type 30 301021 XL - - NDUFB11 - -
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