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Metadata
DOID DOID:0060464
Name Feingold syndrome
Definition An autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.
http://ghr.nlm.nih.gov/condition/feingold-syndrome, http://www.ncbi.nlm.nih.gov/pubmed/?term=14518066, http://www.ncbi.nlm.nih.gov/pubmed/?term=16906565, https://en.wikipedia.org/wiki/Feingold_syndrome
Xrefs

ICD10CM:Q87.8

MESH:C537734

OMIM:164280

OMIM:614326

ORDO:1305

Subsets

DO_rare_slim

Synonyms

digital anomalies with short palpebral fissures and atresia of esophagus or duodenum [EXACT]

FGLDS [EXACT]

microcephaly-digital anomalies-normal intelligence syndrome [EXACT]

microcephaly-oculo-digito-esophageal-duodenal syndrome [EXACT]

MODED syndrome [EXACT]

oculo-digito-esophageal-duodenal syndrome [EXACT]

ODED syndrome [EXACT]

Relationships

is_a autosomal dominant disease

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