DISEASES

Disease-gene associations mined from literature

Human genes for branchiooculofacial syndrome

Branchiooculofacial syndrome [DOID:0050691]

An autosomal dominant disease that is characterized by low birth weight and growth retardation, bilateral branchial clefts.

Synonyms:  branchiooculofacial syndrome,  DOID:0050691,  branchiooculofacial disease,  branchiooculofacial disorder

Linkouts:  OMIM