DISEASES

Disease-gene associations mined from literature

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Human genes for cataract 9 multiple types

Cataract 9 multiple types [DOID:0110266]

A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.

Synonyms:  cataract 9 multiple types,  DOID:0110266,  cataract 9 multiple types with or without microcornea,  CTRCT9,  autosomal recessive congenital cataract 1 ...

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.