DISEASES

Disease-gene associations mined from literature

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Human genes for Meier-Gorlin syndrome

Meier-Gorlin syndrome [DOID:0060306]

A syndrome that is characterized by bilateral underdevelopment of the external ear, short stature, absent or underdeveloped patellae and severe prenatal and postnatal growth retardation.

Synonyms:  Meier-Gorlin syndrome,  DOID:0060306,  MeierGorlin syndrome,  Meier-Gorlin disease,  Meier-Gorlin disorder ...

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.