Neurofibrosarcoma

Symptom Information:

Symptom ID: HPO:0100697
Synonyms:
Malignant peripheral nerve sheath tumor [HPO:0100697]
Malignant schwannoma [HPO:0100697]
Neurosarcoma [HPO:0100697]
Malignant schwannoma [OMIM:Malignant schwannoma]
Neurofibrosarcoma [OMIM:Neurofibrosarcoma]
Malignant peripheral nerve sheath tumors [OMIM:Malignant peripheral nerve sheath tumors]
Malignant peripheral nerve sheath tumors (21%) [OMIM:Malignant peripheral nerve sheath tumors (21%)]
Neurofibrosarcomas [MedDRA:10029273]
Neurofibrosarcoma [MedDRA:10061527]
Quality:
Cross references:
OMIM: "Malignant schwannoma" [OMIM:Malignant schwannoma]
OMIM: "Neurofibrosarcoma" [OMIM:Neurofibrosarcoma]
OMIM: "Malignant peripheral nerve sheath tumors" [OMIM:Malignant peripheral nerve sheath tumors]
OMIM: "Malignant peripheral nerve sheath tumors (21%)" [OMIM:Malignant peripheral nerve sheath tumors (21%)]
Is a (Direct Parents):
HPO         Sarcoma
MedDRA Soft tissue neoplasms malignant and unspecified
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by histology(HPO:0011792)
             Sarcoma(HPO:0100242)
                Neurofibrosarcoma(HPO:0100697)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Soft tissue neoplasms malignant and unspecified(MedDRA:10072990)
       Neurofibrosarcoma(HPO:0100697)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
NOONAN SYNDROME 1 (OMIM:163950)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Noonan syndrome (Orphanet:648)