DISEASES

Disease-gene associations mined from literature

Human genes for Feingold syndrome

Feingold syndrome [DOID:0060464]

A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.

Synonyms:  Feingold syndrome,  DOID:0060464,  Feingold disease,  Feingold disorder,  Feingold syndromes ...