|OBO ID: DOID:0060464|
|Term Name:||Feingold syndrome||Search Ontology:|
|Definition:||A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. (4)|
|Ontology:||Human Disease (DOID:0060464)|
|is a type of:||
OTHER Feingold syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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