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
04505 CAGSSS cataracts?, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia (CAGSSS) 616007 AR 7 7 IARS2 - -
06810 GRIDHH Growth retardation, impaired intellectual development, hypotonia, and hepatopathy 617093 AR - - IARS - -
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