DISEASES

Disease-gene associations mined from literature

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Human genes for autosomal dominant hypocalcemia

Autosomal dominant hypocalcemia [DOID:0090109]

A metal metabolism disorder characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone.

Synonyms:  autosomal dominant hypocalcemia,  autosomal dominant hypocalcemias,  DOID:0090109,  HYPOC,  HYPOCs

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.