Term info
database cross reference
- Orphanet:488647 (MONDO:equivalentTo)
- OMIM:616871 (Orphanet:488647)
Subsets
ordo_disease
definition
Any hereditary neoplastic syndrome in which the cause of the disease is a mutation in the DDX41 gene.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_488647, https://omim.org/entry/616871
has exact synonym
DDX41 hereditary neoplastic syndrome, DDX41-related hematologic malignancy predisposition syndrome, hereditary neoplastic syndrome caused by mutation in DDX41, myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to, MPLPF
has related synonym
susceptibility to familial (multiple types) myeloproliferative/lymphoproliferative neoplasms
id
MONDO:0014809