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Feingold Syndrome Type 1 (MONDO:0008115)

Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.

Overview

Category

Ontology ID

Internal:9431

Synonyms

Brunner-Winter syndrome type 1

FGLDS1

FS1

Feingold syndrome caused by mutation in MYCN

Feingold syndrome type 1

MMT type 1

MODED syndrome type 1

MYCN Feingold syndrome

ODED syndrome type 1

digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1

digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1

microcephaly-digital anomalies-normal intelligence syndrome type 1

microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1

microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1

oculo-digito-esophageal-duodenal syndrome type 1

Feingold syndrome

Feingold syndrome 1

Mmt syndrome

Oded syndrome

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

digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum

microcephaly and digital abnormalities with normal intelligence

microcephaly, intellectual disability, and tracheoesophageal fistula syndrome

microcephaly, mental retardation, and tracheoesophageal fistula syndrome

microcephaly-oculo-digito-esophageal-duodenal syndrome

oculodigitoesophagoduodenal syndrome

Mapped terms

GARD:0017624

ICD9:759.89

MEDGEN:1637716

OMIM:164280

Orphanet:391641

SCTID:702431004

UMLS:C4551774

Child terms

Unknown children.