ZFIN Human Disease: Feingold syndrome

OBO ID: DOID:0060464

Term Name:	Feingold syndrome		Search Ontology:
Synonyms:	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:	GARD:8407 ICD10CM:Q87.8 MESH:C537734 OMIM:164280 OMIM:614326 ORDO:1305
Ontology:	Human Disease ( DOID:0060464 )

Relationships

is a type of:	autosomal dominant disease syndrome autosomal dominant disease syndrome Show first 5 Terms

OTHER Feingold syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYCN	mycn	Feingold syndrome 1	164280

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None