Short stature, impaired intellectual development, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting

Preferred Label : Short stature, impaired intellectual development, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Short stature, mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting;

Prefixed ID : %605856;

Détails

Origin ID

605856;

UMLS CUI

C1970039;

Automatic exact mappings (from CISMeF team)
- short stature, mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting [MeSH concept]
Currated CISMeF NLP mapping
- short stature, mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- short stature, mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting [MeSH Supplementary Concept]
- short stature, mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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