A developmental brain abnormality characterized by an excessive amount of small convolutions on the surface of the brain and cognitive dysfunction. [ NCIT:C116936 ]

This is just here as a test because I lose it

Term information

database cross reference
  • icd11.foundation:2081858551 (Orphanet:35981)
  • MEDGEN:78605 (MONDO:equivalentTo)
  • MESH:D065706 (MONDO:equivalentTo)
  • GARD:18818 (MONDO:GARD)
  • NANDO:1201071 (https://orcid.org/0000-0003-0011-764X)
  • UMLS:C0266464 (MONDO:equivalentTo)
  • DOID:0080918 (MONDO:equivalentTo)
  • NCIT:C116936 (MONDO:equivalentTo)
  • Orphanet:35981 (MONDO:equivalentTo)
  • SCTID:4945003 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/NCIT_C116936

http://identifiers.org/snomedct/4945003

http://www.orpha.net/ORDO/Orphanet_35981

http://identifiers.org/medgen/78605

http://identifiers.org/mesh/D065706

http://linkedlifedata.com/resource/umls/id/C0266464

http://purl.obolibrary.org/obo/DOID_0080918

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0000508

id

MONDO:0000087

Term relations