Terminology Service for NFDI4Health
Feingold Syndrome
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http://purl.obolibrary.org/obo/NCIT_C74987
A rare autosomal dominant syndrome caused by mutations in the MYCN oncogene. It is characterized by microcephaly, limb abnormalities, esophageal and/or duodenal atresia. [ ]
Term info
Label
Feingold Syndrome
Synonyms
- Feingold Syndrome
Legacy Concept Name
Feingold_Syndrome
Preferred Name
Feingold Syndrome
Semantic Type
Disease or Syndrome
UMLS CUI
C0796068
code
C74987