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DO Term : Feingold syndrome [DOID:0060464] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
164280,
614326,
MESH:C537734,
microcephaly-oculo-digito-esophageal-duodenal syndrome,
GARD:8407,
microcephaly-digital anomalies-normal intelligence syndrome,
OMIM:614326,
ODED syndrome,
OMIM:164280,
digital anomalies with short palpebral fissures and atresia of esophagus or duodenum,
ORDO:1305,
oculo-digito-esophageal-duodenal syndrome,
MODED syndrome,
FGLDS,
ICD10CM:Q87.8

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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