autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
http://purl.obolibrary.org/obo/MONDO_0018446
Term info
database cross reference
- Orphanet:404481 (MONDO:equivalentTo)
- UMLS:CN226191 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/5588
exactMatch
http://linkedlifedata.com/resource/umls/id/CN226191, http://purl.obolibrary.org/obo/Orphanet_404481
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0000508
id
MONDO:0018446