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
04589 CLIFAHDD contractures, limbs and face, congenital, hypotonia, and developmental delay (CLIFAHDD) 616266 AD 2 1 NALCN - -
03937 IHPRF1 hypotonia, infantile, with psychomotor retardation and characteristic facies, type 1 (IHPRF-1) 615419 AR 5 4 NALCN - -
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