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Diseases

pineoblastoma

pineoblastoma

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
pineoblastoma
Standard Disease Name
pineoblastoma
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D010871
OMIM ID
No data
UMLS ID
C0205898
HPO ID
No data

Description and Extensions

Description
NCI2016_NCI-GLOSS_1602D:A fast growing type of brain tumor that occurs in or around the pineal gland, a tiny organ near the center of the brain.|NCI2016_CDISC_1602D:A poorly differentiated malignant embryonal neoplasm arising from the pineal region of the brain.|NCI2016_02D:A poorly differentiated malignant embryonal neoplasm arising from the pineal region. It usually occurs in children and it is characterized by the presence of small immature neuroepithelial cells. It may follow an aggressive clinical course.|HPO2016_07_04:Pineoblastoma is a rare primitive neuroectodermal tumour (PNET) arising in the pineal gland. Pineoblastomas are classified as a WHO grade IV tumour and comprise one-fourth to one-half of pineal parenchymal tumours. Pineoblastoma is a highly cellular tumor originating in the pineal gland and containing small, poorly differentiated cells. [HPO:probinson] {comment="PMID:21717450"}
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
03
MYC
MYC proto-oncogene, bHLH transcription factor
MYC proto-oncogene, bHLH transcription factor
04
MYCN
MYCN proto-oncogene, bHLH transcription factor
MYCN proto-oncogene, bHLH transcription factor
06
PDE4DIP
phosphodiesterase 4D interacting protein
phosphodiesterase 4D interacting protein
07
RB1
RB transcriptional corepressor 1
RB transcriptional corepressor 1