OBO ID: DOID:0060464 |
Term Name: | Feingold syndrome | Search Ontology: | |
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Definition: | A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. (4) | ||
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Ontology: | Human Disease ( DOID:0060464 ) |
OTHER Feingold syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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