Term info
database cross reference
- UMLS:CN226095 (MONDO:equivalentTo)
- Orphanet:398079 (MONDO:equivalentTo)
Subsets
ordo_clinical_subtype
A synonym that is historic and discouraged
Prader-Willi-like syndrome due to a point mutation
[
Orphanet:398079
]
exactMatch
http://purl.obolibrary.org/obo/Orphanet_398079, http://linkedlifedata.com/resource/umls/id/CN226095
has exact synonym
SIM1-related PWLS
has related synonym
PWS-like due to a point mutation, PWS-like due to point mutation, Prader-Willi-like syndrome due to a point mutation
id
MONDO:0018355