DISEASES - autosomal dominant non-syndromic intellectual disability 41

Human genes for autosomal dominant non-syndromic intellectual disability 41

Autosomal dominant non-syndromic intellectual disability 41 [DOID:0070071]

An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of TBL1XR1 on chromosome 3q26.32.

Synonyms: autosomal dominant non-syndromic intellectual disability 41, DOID:0070071, autosomal dominant nonsyndromic intellectual disability 41, MRD41, autosomal dominant mental retardation 41

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.