Search Ontology:
Human Disease
Feingold syndrome
- Term ID
- DOID:0060464
- Synonyms
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- digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
- FGLDS
- microcephaly-digital anomalies-normal intelligence syndrome
- microcephaly-oculo-digito-esophageal-duodenal syndrome
- MODED syndrome
- oculo-digito-esophageal-duodenal syndrome
- ODED syndrome
- Definition
- A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. (4)
- References
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- GARD:8407
- ICD10CM:Q87.8
- MESH:C537734
- MIM:164280
- MIM:614326
- ORDO:1305
- Ontology
- Human Disease ( DOID:0060464 )
- is a type of
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Genes Involved
Zebrafish Models