Plexiform neurofibroma

Symptom Information:

Symptom ID: HPO:0009732
Synonyms:
Plexiform neurofibroma [OMIM:Plexiform neurofibroma]
Plexiform neurofibroma (76%) [OMIM:Plexiform neurofibroma (76%)]
Quality:
Cross references:
OMIM: "Plexiform neurofibroma" [OMIM:Plexiform neurofibroma]
OMIM: "Plexiform neurofibroma (76%)" [OMIM:Plexiform neurofibroma (76%)]
Is a (Direct Parents):
HPO         Neurofibromas
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Neoplasm of the nervous system(HPO:0004375)
             Neoplasm of the peripheral nervous system(HPO:0100007)
                Neurofibromas(HPO:0001067)
                   Plexiform neurofibroma(HPO:0009732)
          Abnormality of nervous system morphology(HPO:0012639)
             Abnormal peripheral nervous system morphology(HPO:0000759)
                Neoplasm of the peripheral nervous system(HPO:0100007)
                   Neurofibromas(HPO:0001067)
                      Plexiform neurofibroma(HPO:0009732)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skin(HPO:0008069)
                Neurofibromas(HPO:0001067)
                   Plexiform neurofibroma(HPO:0009732)
             Neoplasm of the nervous system(HPO:0004375)
                Neoplasm of the peripheral nervous system(HPO:0100007)
                   Neurofibromas(HPO:0001067)
                      Plexiform neurofibroma(HPO:0009732)
          Neoplasm by histology(HPO:0011792)
             Fibrous tissue neoplasm(HPO:0012316)
                Fibroma(HPO:0010614)
                   Neurofibromas(HPO:0001067)
                      Plexiform neurofibroma(HPO:0009732)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Neoplasm of the skin(HPO:0008069)
                Neurofibromas(HPO:0001067)
                   Plexiform neurofibroma(HPO:0009732)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)