All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02697 - Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive 607706 AR 4 3 GDAP1 - -
02709 CMT2K Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K 607831 AD;AR 7 5 GDAP1, JPH1 - -
01705 CMT4A Charcot-Marie-Tooth disease, type 4A (CMT-4A) 214400 AR 25 25 GDAP1 - -
02752 CMTRIA Charcot-Marie-Tooth disease, recessive intermediate A (CMTRIA) 608340 AR - - GDAP1 - -
00616 PRLTS Perrault syndrome - - 32 32 C10orf12, CLPP, DAP3, ERAL1, HARS2, HSD17B4, LARS2 - -
06050 SCAR27 Spinocerebellar ataxia, autosomal recessive 27 618369 AR - - GDAP2 - -
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