pachygyria, frontotemporal

Preferred Label : pachygyria, frontotemporal;

MeSH synonym : autosomal recessive frontotemporal pachygyria;

Origin ID

C538092;

UMLS CUI

C1853215;

Currated CISMeF NLP mapping
- Autosomal recessive frontotemporal pachygyria [ORDO Disease]
- Autosomal recessive frontotemporal pachygyria (disorder) [SNOMED CT concept]
- Pachygyria, frontotemporal [OMIM Phenotype]
MeSH term(s) associated for indexing
- lissencephaly [MeSH Descriptor]
Record concept(s)
- pachygyria, frontotemporal [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive frontotemporal pachygyria [ORDO Disease]
- Autosomal recessive frontotemporal pachygyria (disorder) [SNOMED CT concept]
- Pachygyria, frontotemporal [OMIM Phenotype]