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
06364 CHN3 Hypomyelinating neuropathy, congenital, 3 618186 AR - - CNTNAP1 - -
04418 LCCS7 contracture syndrome, lethal, congenital, type 7 (LCCS-7) 616286 AR 1 1 CNTNAP1 - -
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