A developmental brain abnormality characterized by an excessive amount of small convolutions on the surface of the brain and cognitive dysfunction. [ NCIT:C116936 ]
Term information
- 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)
gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders
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