Medulloblastoma

Symptom Information:

Symptom ID: HPO:0002885
Synonyms:
Medulloblastoma (disorder) [Orphanet:50960]
Medulloblastoma, no ICD-O subtype (morphologic abnormality) [Orphanet:50960]
medulloblastoma [HPO:0002885]
Medulloblastoma [Orphanet:50960]
Medulloblastoma [OMIM:Medulloblastoma]
Medulloblastoma [MedDRA:10027107]
Quality:
Cross references:
Orphanet:50960 "Medulloblastoma" [Orphanet:50960]
OMIM: "Medulloblastoma" [OMIM:Medulloblastoma]
UMLS:C0025149 "medulloblastoma" [HPO:0002885]
UMLS:C0025149 "Medulloblastoma" [Orphanet:50960]
Is a (Direct Parents):
Orphanet Neoplasm of the central nervous system
HPO         Malignant neoplasm of the central nervous system
MedDRA Glial tumours malignant
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)
                      Medulloblastoma(HPO:0002885)
       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)
                   Medulloblastoma(HPO:0002885)
          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)
                      Medulloblastoma(HPO:0002885)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Nervous system neoplasms malignant and unspecified NEC(MedDRA:10029211)
       Glial tumours malignant(MedDRA:10018335)
          Medulloblastoma(HPO:0002885)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

APC-related attenuated familial adenomatous polyposis (Orphanet:247806)
Attenuated familial adenomatous polyposis (Orphanet:220460)
Atypical teratoid tumor (Orphanet:99966)
Classic medulloblastoma (Orphanet:251867)
Constitutional mismatch repair deficiency syndrome (Orphanet:252202)
Desmoplastic/nodular medulloblastoma (Orphanet:251863)
FANCONI ANEMIA, COMPLEMENTATION GROUP N (OMIM:610832)
Familial adenomatous polyposis (Orphanet:733)
Familial rhabdoid tumor (Orphanet:231108)
Gardner syndrome (Orphanet:79665)
Gorlin syndrome (Orphanet:377)
Medulloblastoma (Orphanet:616)
Medulloblastoma with extensive nodularity (Orphanet:251858)
Melanoma and neural system tumor syndrome (Orphanet:252206)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Nijmegen breakage syndrome (Orphanet:647)
Non-polyposis Turcot syndrome (Orphanet:99817)
Pleuropulmonary blastoma (Orphanet:64742)
Pleuropulmonary blastoma family tumor susceptibility syndrome (Orphanet:284343)
Turcot syndrome with polyposis (Orphanet:99818)