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Diseases

Atypical Teratoid/Rhabdoid Tumor

atypical teratoid/rhabdoid tumor

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
Atypical Teratoid/Rhabdoid Tumor
Standard Disease Name
atypical teratoid/rhabdoid tumor
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
609322
UMLS ID
C1266184
HPO ID
No data

Description and Extensions

Description
NCI2016_NCI-GLOSS_1602D:An aggressive cancer of the central nervous system, kidney, or liver that occurs in very young children.|NCI2016_02D:An aggressive malignant embryonal neoplasm arising from the central nervous system. It is composed of cells with a large eccentric nucleus, prominent nucleolus, and abundant cytoplasm. It may be associated with loss of chromosome 22. The vast majority of cases occur in childhood. Symptoms include lethargy, vomiting, cranial nerve palsy, headache, and hemiplegia.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
06
GFAP
glial fibrillary acidic protein
glial fibrillary acidic protein
08
IGF1R
insulin like growth factor 1 receptor
insulin like growth factor 1 receptor