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 ...