Microcephaly with simplified gyral pattern

Preferred Label : Microcephaly with simplified gyral pattern;

Type : Phenotype or locus, molecular basis unknown;

Prefixed ID : %603802;

Details

Origin ID

603802;

UMLS CUI

C1863516;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive primary microcephaly [ORDO Disease]
Currated CISMeF NLP mapping
- Microcephaly with simplified gyral pattern (disorder) [SNOMED CT concept]
- microcephaly with simplified gyral pattern [MeSH concept]
- microcephaly with simplified gyral pattern [MeSH Supplementary Concept]
ORDO concept(s)
- Autosomal recessive primary microcephaly [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Microcephaly with simplified gyral pattern (disorder) [SNOMED CT concept]
- microcephaly with simplified gyral pattern [MeSH Supplementary Concept]
- microcephaly with simplified gyral pattern [MeSH concept]

Keyword's position in hierarchy(ies) :

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