DISEASES

Disease-gene associations mined from literature

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Human genes for orofacial cleft 1

Orofacial cleft 1 [DOID:0080395]

An orofacial cleft characterized by autosomal dominant inheritance that has_material_basis_in variation in chromosome region 6p24.3.

Synonyms:  orofacial cleft 1,  DOID:0080395,  nonsyndromic cleft lip with or without cleft palate 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.