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
07251 CMYO26 myopathy, congenital, type 26 621225 AD - - TUBA4A - -
05049 FTDALS9;ALS22 dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 9 616208 AD - - TUBA4A - -
07252 OZEMA23 oocyte/zygote/embryo maturation arrest, type 23 621231 AD;AR - - TUBA4A - -
07253 SPAX11 ataxia, spastic, type 11, autosomal dominant 621226 AD - - TUBA4A - -
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