All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05614 DYTOABG dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities (DYTOABG) 617282 AR - - MECR - autosomal recessive
06854 MFHIEN Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis 300990 XLR - - AMMECR1 - -
07051 OPA16 atrophy, optic, type 16 620629 - - - MECR - -
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