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
07205 CONDCAC nurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline 620636 AD - - CAPRIN1 - -
05611 NDD neurodevelopmental disorder (NDD) - - 4415 4235 ACBD6, ADARB1, AP1G1, ARFGEF1, ATP9A, CAMK2D, CAMSAP1, CAPRIN1, CASP2, CHASERR, CLCN3, CPSF3L, DDB1, DENND5B, DHX30, DHX9, DOHH, DOT1L, EEFSEC, EIF2C1, 91 more - -
07206 NEDLAAD neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder 620782 AD - - CAPRIN1 - -
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