microlissencephaly

Preferred Label : microlissencephaly;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0502928;

UMLS CUI

C1956147;

Automatic exact mappings (from CISMeF team)
- Microlissencephaly [ICD-11 More detail]
- Microlissencephaly [HPO term]
Currated CISMeF NLP mapping
- Microlissencephaly [ORDO Disease]
- Microlissencephaly (disorder) [SNOMED CT concept]
False automatic mappings
- Lissencephaly syndrome, Norman-Roberts type [ORDO Disease]
Related record
- microcephaly [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Microlissencephaly [ORDO Disease]
- Microlissencephaly [HPO term]
- Microlissencephaly (disorder) [SNOMED CT concept]