All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06562 CMT2T Charcot-Marie-Tooth disease, axonal, type 2T 617017 AD;AR - - MME - -
04580 MBNP glomerulonephritis, membranous, antenatal (MBNP) 614692 - - - MME - -
06854 MFHIEN Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis 300990 XLR - - AMMECR1 - -
06563 SCA43 ?Spinocerebellar ataxia 43 617018 AD - - MME - -
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