Term info
database cross reference
- Orphanet:294949 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
comment
some subtypes may be syndromic eg congenital radioulnar synostosis
exactMatch
http://purl.obolibrary.org/obo/Orphanet_294949
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0015227
id
MONDO:0017429