DISEASES - autosomal dominant intellectual developmental disorder 10

Human genes for autosomal dominant intellectual developmental disorder 10

Autosomal dominant intellectual developmental disorder 10 [DOID:0070040]

An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of CACNG2 on chromosome 22q12.3.

Synonyms: autosomal dominant intellectual developmental disorder 10, DOID:0070040, autosomal dominant mental retardation 10, autosomal dominant non-syndromic intellectual disability 10, MRD10 ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.