DISEASES

Disease-gene associations mined from literature

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Human genes for neurodegeneration with brain iron accumulation 3

Neurodegeneration with brain iron accumulation 3 [DOID:0110737]

A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33.

Synonyms:  neurodegeneration with brain iron accumulation 3,  DOID:0110737,  Neuroferritinopathy,  Adult basal ganglia disease,  Ferritin-related neurodegeneration ...

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.