Meningioma

Symptom Information:

Symptom ID: HPO:0002858
Synonyms:
Meligioma [HPO:0002858]
Mengioma [HPO:0002858]
Mengiomia [HPO:0002858]
Menigiom [HPO:0002858]
Menigioma [HPO:0002858]
Meningioma, benign, no ICD-O subtype (morphologic abnormality) [Orphanet:50970]
Meningioma, benign, no ICD-O subtype [Orphanet:50970]
Meningioma [Orphanet:50970]
Meningioma [OMIM:Meningioma]
Meningioma [MedDRA:10027191]
Multiple meningioma [MedDRA:10027191]
Meningiomas [OMIM:Meningiomas]
Quality:
Cross references:
Orphanet:50970 "Meningioma" [Orphanet:50970]
OMIM: "Meningioma" [OMIM:Meningioma]
OMIM: "Meningiomas" [OMIM:Meningiomas]
UMLS:C1762616 "Meningioma" [HPO:0002858]
UMLS:C1762616 "Meningioma, benign, no ICD-O subtype" [Orphanet:50970]
UMLS:C0025286 "Meningioma" [Orphanet:50970]
Is a (Direct Parents):
HPO         Benign neoplasm of the central nervous system
MedDRA Nervous system neoplasms unspecified malignancy NEC
Orphanet Neoplasm of the central nervous system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the nervous system(HPO:0004375)
                Neoplasm of the central nervous system(HPO:0100006)
                   Benign neoplasm of the central nervous system(HPO:0100835)
                      Meningioma(HPO:0002858)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Neoplasm of the central nervous system(HPO:0100006)
                   Benign neoplasm of the central nervous system(HPO:0100835)
                      Meningioma(HPO:0002858)
          Neoplasm of the nervous system(HPO:0004375)
             Neoplasm of the central nervous system(HPO:0100006)
                Benign neoplasm of the central nervous system(HPO:0100835)
                   Meningioma(HPO:0002858)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Nervous system neoplasms malignant and unspecified NEC(MedDRA:10029211)
       Nervous system neoplasms unspecified malignancy NEC(MedDRA:10029213)
          Meningioma(HPO:0002858)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
BAP1-related tumor predisposition syndrome (Orphanet:289539)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
COWDEN SYNDROME 5 (OMIM:615108)
COWDEN SYNDROME 6 (OMIM:615109)
Cowden syndrome (Orphanet:201)
Familial multiple meningioma (Orphanet:263662)
Gorlin syndrome (Orphanet:377)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
LI-FRAUMENI SYNDROME 2 (OMIM:609265)
Lhermitte-Duclos disease (Orphanet:65285)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Melanoma and neural system tumor syndrome (Orphanet:252206)
NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL (OMIM:162260)
Neurocutaneous melanocytosis (Orphanet:2481)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Neurofibromatosis type 2 (Orphanet:637)
Neurofibromatosis type 3 (Orphanet:93921)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
SCHWANNOMATOSIS 1 (OMIM:162091)
Werner syndrome (Orphanet:902)