Terminology Service for NFDI4Health

Cornelia De Lange Syndrome

Go to external page http://purl.obolibrary.org/obo/NCIT_C75016


A rare syndrome characterized by low birth weight, delayed growth, mental retardation, behavioral problems, and a distinctive facial appearance (thin, arched eyebrows, low set ears, small teeth, and small nose). The majority of cases are caused by mutations in the NIPBL gene. Less severe forms of the syndrome are caused by mutations in the SMC1A and SMC3 genes. [ ]

Term info

Label

Cornelia De Lange Syndrome

Synonyms
  • Cornelia De Lange Syndrome
Subsets

NCIT_C99147, NCIT_C90259

Has NICHD Parent

http://purl.obolibrary.org/obo/NCIT_C3101, http://purl.obolibrary.org/obo/NCIT_C89330

Legacy Concept Name

Cornelia_De_Lange_Syndrome

NICHD Hierarchy Term

Cornelia De Lange Syndrome

Preferred Name

Cornelia De Lange Syndrome

Semantic Type

Disease or Syndrome

UMLS CUI

C0270972

code

C75016