All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04130 FTDALS-2 dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 2 (FTDALS-2) 615911 - 0 0 CHCHD10 - -
04408 IMMD myopathy?, isolated mitochondrial, autosomal dominant(IMMD) 616209 - 0 0 CHCHD10 - -
04409 SMAJ atrophy, muscular, spinal, Jokela type (SMAJ) 615048 - 0 0 CHCHD10 - -
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