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Results: 1 to 20 of 24

1.

Rhabdomyosarcoma

A malignant mesenchymal neoplasm arising from skeletal muscle. [from NCI]

MedGen UID:
20561
Concept ID:
C0035412
Neoplastic Process
2.

Embryonal rhabdomyosarcoma

MedGen UID:
505967
Concept ID:
CN005870
Finding
3.

Rhabdomyosarcoma

MedGen UID:
505375
Concept ID:
CN002584
Finding
4.

Rhabdomyosarcoma, Embryonal

A form of RHABDOMYOSARCOMA arising primarily in the head and neck, especially the orbit, of children below the age of 10. The cells are smaller than those of other rhabdomyosarcomas and are of two basic cell types: spindle cells and round cells. This cancer is highly sensitive to chemotherapy and has a high cure rate with multi-modality therapy. (From Holland et al., Cancer Medicine, 3d ed, p2188) [from MeSH]

MedGen UID:
104910
Concept ID:
C0206656
Neoplastic Process
5.

Detected

MedGen UID:
617726
Concept ID:
C0442726
Finding
6.

specific processes that generate the ability of an organism to cause disease [from CHV]

MedGen UID:
195936
Concept ID:
C0699748
7.

Finding

The result of an examination or inquiry. [from NCI]

MedGen UID:
66215
Concept ID:
C0243095
Finding
8.

Clinical finding

clinical manifestations that can be either objective when observed by a physician, or subjective when perceived by the patient. [from CRISP]

MedGen UID:
19974
Concept ID:
C0037088
Sign or Symptom
9.

Sarcoma

A malignant mesenchymal neoplasm. A general term for which the transformed cell type has not been specified. [from NCI]

MedGen UID:
224714
Concept ID:
C1261473
Neoplastic Process
10.

Epithelioid sarcoma

An aggressive malignant neoplasm of uncertain lineage, characterized by the presence of epithelioid cells forming nodular patterns. The nodules often undergo central necrosis, resulting in a pseudogranulomatous growth pattern. It usually occurs in young adults. The most common sites of involvement are the extremities (distal-type epithelioid sarcoma), and less frequently the pelvis, perineum, and genital organs (proximal-type epithelioid sarcoma). [from NCI]

MedGen UID:
104753
Concept ID:
C0205944
Neoplastic Process
11.

Mutagenesis Process

Process of generating a genetic MUTATION. It may occur spontaneously or be induced by MUTAGENS. [from MeSH]

MedGen UID:
86969
Concept ID:
C0079866
Molecular Function
12.

Myofibroblastoma

A benign, well circumscribed soft tissue neoplasm characterized by the presence of spindle shaped myofibroblasts and mast cells in a collagenous stroma. [from NCI]

MedGen UID:
66894
Concept ID:
C0242404
Neoplastic Process
13.

Connective and Soft Tissue Neoplasm

Neoplasms developing from some structure of the connective and subcutaneous tissue. The concept does not refer to neoplasms located in connective or soft tissue. [from MeSH]

MedGen UID:
60224
Concept ID:
C0206765
Neoplastic Process
14.

Neoplasms, Muscle Tissue

Neoplasms composed of muscle tissue: skeletal, cardiac, or smooth. The concept does not refer to neoplasms located in muscles. [from MeSH]

MedGen UID:
45037
Concept ID:
C0027664
Neoplastic Process
15.

Myosarcoma

A general term for a malignant neoplasm derived from muscular tissue. (Stedman, 25th ed) [from MeSH]

MedGen UID:
44559
Concept ID:
C0027095
Neoplastic Process
16.

Myoblastoma

A granular cell tumor that is confined to the site of origin, without metastatic potential. [from NCI]

MedGen UID:
44550
Concept ID:
C0027043
Neoplastic Process
17.

Chromosomal translocation

Any type of genetic recombination involving exchange of DNA between non-homologous chromosomes, which often occurs as the result of non-homologous end-joining of broken DNA strands. Chromosomal translocation is involved in repairing broken DNA and in maintaining cell viability at the expense of long term genomic stability. This process is is associated with particular types of leukemia, infertility and Down Syndrome. [from NCI]

MedGen UID:
21243
Concept ID:
C0040715
Cell or Molecular Dysfunction
18.

Neoplasms by Histologic Type

A collective term for the various histological types of NEOPLASMS. It is more likely to be used by searchers than by indexers and catalogers. [from MeSH]

MedGen UID:
10295
Concept ID:
C0027652
Neoplastic Process
19.

Chromosome Aberrations

irregularity in the number or structure of chromosomes that may alter the course of development. [from CRISP]

MedGen UID:
954
Concept ID:
C0008625
Cell or Molecular Dysfunction
20.

Rhabdomyosarcoma, embryonal, 2

MedGen UID:
357232
Concept ID:
C1867234
Disease or Syndrome

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