Disease-gene associations mined from literature

Human genes for Goldenhar syndrome

Goldenhar syndrome [DOID:2907]

A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch.

Synonyms:  Goldenhar syndrome,  DOID:2907,  Goldenhar disease,  Goldenhar disorder,  Goldenhar syndromes ...

Linkouts:  OMIM