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
06529 HMSN6C Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy 618511 AR - - PDXK - -
02190 MCLDS McLeod syndrome (neuroacanthocytosis) 300842 XL 26 21 XK - -
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