neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
http://purl.obolibrary.org/obo/MONDO_0018208
Term info
database cross reference
- Orphanet:363700 (MONDO:equivalentTo)
- UMLS:CN204726 (MONDO:equivalentTo)
Subsets
ordo_etiological_subtype
exactMatch
http://linkedlifedata.com/resource/umls/id/CN204726, http://purl.obolibrary.org/obo/Orphanet_363700
has exact synonym
Von Recklinghausen disease due to NF1 mutation or intragenic deletion
id
MONDO:0018208