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
01138 OPTB8 osteopetrosis, autosomal recessive, type 8 615085 AR - - SNX10 - -
04669 SCAR20 ataxia, spinocerebellar, autosomal recessive, type 20 (SCAR-20) 616354 AR 4 3 SNX14 - -
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