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Results: 8

1.

Rhabdoid Tumor

A malignant tumor of either the central nervous system (CNS) or the kidney. Malignant rhabdoid tumors of the CNS often have an abnormality of chromosome 22. These tumors usually occur in children younger than 2 years. [from NCI_NCI-GLOSS]

MedGen UID:
64646
Concept ID:
C0206743
Neoplastic Process
2.

Atypical teratoid/rhabdoid tumor

MedGen UID:
799292
Concept ID:
CN201964
Disease or Syndrome
3.

Atypical teratoid rhabdoid tumor

Atypical teratoid rhabdoid tumor (ATRT) is a highly malignant central nervous system (CNS) rhabdoid tumor (RT; see this term) found almost exclusively in children. [from ORDO]

MedGen UID:
798196
Concept ID:
CN207484
Disease or Syndrome
4.

Malignant rhabdoid tumor, somatic

MedGen UID:
442465
Concept ID:
C2750405
Disease or Syndrome
5.

Atypical Teratoid/Rhabdoid Tumor

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. [from NCI]

MedGen UID:
226853
Concept ID:
C1266184
Neoplastic Process
6.

Proliferation

Growth and reproduction of new similar forms, e.g. cells, buds, or offspring. [from NCI]

MedGen UID:
137720
Concept ID:
C0334094
Pathologic Function
7.

Inhibition

MedGen UID:
5809
Concept ID:
C0021469
Molecular Function
8.

Malignant neoplasm of the central nervous system

A primary or metastatic malignant neoplasm involving the brain or spinal cord. Representative examples include anaplastic astrocytoma, glioblastoma, anaplastic (malignant) meningioma, lymphoma, and metastatic carcinoma from another anatomic site. [from NCI]

MedGen UID:
87593
Concept ID:
C0348374
Neoplastic Process

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