Astrocytoma

Symptom Information:

Symptom ID: HPO:0009592
Synonyms:
Astrocytoma [OMIM:Astrocytoma]
Astrocytomas [OMIM:Astrocytomas]
Astrocytoma [MedDRA:10003571]
Quality:
Cross references:
OMIM: "Astrocytoma" [OMIM:Astrocytoma]
OMIM: "Astrocytomas" [OMIM:Astrocytomas]
UMLS:C0004114 "Astrocytoma" [HPO:0009592]
Is a (Direct Parents):
HPO         Glioma
MedDRA Nervous system neoplasms unspecified malignancy NEC
HPO         Abnormality of the astrocytes
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)
                   Malignant neoplasm of the central nervous system(HPO:0100836)
                      Glioma(HPO:0009733)
                         Astrocytoma(HPO:0009592)
       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)
                   Malignant neoplasm of the central nervous system(HPO:0100836)
                      Glioma(HPO:0009733)
                         Astrocytoma(HPO:0009592)
          Neoplasm of the nervous system(HPO:0004375)
             Neoplasm of the central nervous system(HPO:0100006)
                Malignant neoplasm of the central nervous system(HPO:0100836)
                   Glioma(HPO:0009733)
                      Astrocytoma(HPO:0009592)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Nervous system neoplasms malignant and unspecified NEC(MedDRA:10029211)
       Nervous system neoplasms unspecified malignancy NEC(MedDRA:10029213)
          Astrocytoma(HPO:0009592)
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

APC-related attenuated familial adenomatous polyposis (Orphanet:247806)
Astrocytoma (Orphanet:94)
Attenuated familial adenomatous polyposis (Orphanet:220460)
Constitutional mismatch repair deficiency syndrome (Orphanet:252202)
Ependymal tumor (Orphanet:301)
Familial adenomatous polyposis (Orphanet:733)
Gardner syndrome (Orphanet:79665)
Melanoma and neural system tumor syndrome (Orphanet:252206)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Neurofibromatosis type 2 (Orphanet:637)
Non-polyposis Turcot syndrome (Orphanet:99817)
Oligodendroglial tumor (Orphanet:46484)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Tuberous sclerosis (Orphanet:805)
Turcot syndrome with polyposis (Orphanet:99818)