Ependymoma

Symptom Information:

Symptom ID: HPO:0002888
Synonyms:
Ependymoma [OMIM:Ependymoma]
Ependymomas [OMIM:Ependymomas]
Ependymoma [MedDRA:10014967]
Quality:
Cross references:
OMIM: "Ependymoma" [OMIM:Ependymoma]
OMIM: "Ependymomas" [OMIM:Ependymomas]
UMLS:C0014474 "Ependymoma" [HPO:0002888]
Is a (Direct Parents):
HPO         Glioma
MedDRA Nervous system neoplasms unspecified malignancy NEC
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)
                         Ependymoma(HPO:0002888)
       Abnormality of the nervous system(HPO:0000707)
          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)
                      Ependymoma(HPO:0002888)
          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)
                         Ependymoma(HPO:0002888)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Nervous system neoplasms malignant and unspecified NEC(MedDRA:10029211)
       Nervous system neoplasms unspecified malignancy NEC(MedDRA:10029213)
          Ependymoma(HPO:0002888)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Astrocytoma (Orphanet:94)
Constitutional mismatch repair deficiency syndrome (Orphanet:252202)
Ependymal tumor (Orphanet:301)
Glial tumor (Orphanet:182067)
Neurofibromatosis type 2 (Orphanet:637)
Non-polyposis Turcot syndrome (Orphanet:99817)
Oligodendroglial tumor (Orphanet:46484)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Tuberous sclerosis (Orphanet:805)