DISEASES

Disease-gene associations mined from literature

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Human genes for holoprosencephaly 9

Holoprosencephaly 9 [DOID:0110873]

A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.

Synonyms:  holoprosencephaly 9,  DOID:0110873,  holoprosencephaly with microphthalmia and first branchial arch anomalies,  HPE9,  pituitary anomalies with holoprosencephaly-like features ...

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.