Neurofibromas

Symptom Information:

Symptom ID: HPO:0001067
Synonyms:
multiple neurofibromas [HPO:0001067]
Neurofibromata [HPO:0001067]
Neurofibromatosis [HPO:0001067]
Neurofibromas [OMIM:Neurofibromas]
Neurofibromatosis [OMIM:Neurofibromatosis]
Neurofibroma [OMIM:Neurofibroma]
Neurofibromatosis [MedDRA:10029268]
Neurofibroma [MedDRA:10029267]
Quality:
Cross references:
OMIM: "Neurofibromas" [OMIM:Neurofibromas]
OMIM: "Neurofibromatosis" [OMIM:Neurofibromatosis]
OMIM: "Neurofibroma" [OMIM:Neurofibroma]
UMLS:C0027830 "Neurofibromas" [HPO:0001067]
Is a (Direct Parents):
HPO         Neoplasm of the peripheral nervous system
HPO         Neoplasm of the skin
HPO         Fibroma
MedDRA Neurological disorders congenital NEC
MedDRA Nervous system neoplasms benign NEC
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)
          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)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skin(HPO:0008069)
                Neurofibromas(HPO:0001067)
             Neoplasm of the nervous system(HPO:0004375)
                Neoplasm of the peripheral nervous system(HPO:0100007)
                   Neurofibromas(HPO:0001067)
          Neoplasm by histology(HPO:0011792)
             Fibrous tissue neoplasm(HPO:0012316)
                Fibroma(HPO:0010614)
                   Neurofibromas(HPO:0001067)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Neoplasm of the skin(HPO:0008069)
                Neurofibromas(HPO:0001067)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Neurological disorders congenital(MedDRA:10029299)
       Neurological disorders congenital NEC(MedDRA:10029300)
          Neurofibromas(HPO:0001067)
Nervous system disorders(MedDRA:10029205)
    Benign neoplasm of the central nervous system(HPO:0100835)
       Nervous system neoplasms benign NEC(MedDRA:10029210)
          Neurofibromas(HPO:0001067)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Gastrointestinal stromal tumor (Orphanet:44890)
Legius syndrome (Orphanet:137605)
NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME (OMIM:162240)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Neurofibromatosis type 2 (Orphanet:637)
Watson syndrome (Orphanet:3444)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)