All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06854 MFHIEN Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis 300990 XLR - - AMMECR1 - -
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