Microcephaly, facial abnormalities, micromelia, and impaired intellectual development

Preferred Label : Microcephaly, facial abnormalities, micromelia, and impaired intellectual development;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Microcephaly, facial abnormalities, micromelia, and mental retardation;

Prefixed ID : 603572;

Details

Origin ID

603572;

UMLS CUI

C1863702;

Currated CISMeF NLP mapping
- microcephaly, facial abnormalities, micromelia, and mental retardation [MeSH concept]
- microcephaly, facial abnormalities, micromelia, and mental retardation [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- microcephaly, facial abnormalities, micromelia, and mental retardation [MeSH Supplementary Concept]
- microcephaly, facial abnormalities, micromelia, and mental retardation [MeSH concept]

Keyword's position in hierarchy(ies) :

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