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Items: 5

1.

Chordoma

Chordomas are rare, clinically malignant tumors derived from notochordal remnants. They occur along the length of the spinal axis, predominantly in the sphenooccipital, vertebral, and sacrococcygeal regions. They are characterized by slow growth, local destruction of bone, extension into adjacent soft tissues, and, rarely, distant metastatic spread (Stepanek et al., 1998). The incidence of chordoma is age-dependent, with fewer than 5% occurring in children and adolescents (summary by McMaster et al., 2011). [from OMIM]

MedGen UID:
40277
Concept ID:
C0008487
Neoplastic Process
2.

Chordoma

A chordoma is a tumors that arises from embryonic remnants of the notochord along the length of the neuraxis. Chordomas generally occur in the sacrum, intracranially at the clivus, or along the spinal axis. [from HPO]

MedGen UID:
426768
Concept ID:
CN009588
Finding
3.

Parachordoma

A rare, usually benign myoepithelial tumor characterized by the presence of epithelioid, often vacuolated neoplastic cells. Most patients present with painless swelling in the subcutaneous or subfascial soft tissues of the extremities. [from NCI]

MedGen UID:
266108
Concept ID:
C1266175
Neoplastic Process
4.

Axial

Situated on or along or in the direction of an axis.(WordNet) [from NCI]

MedGen UID:
64380
Concept ID:
C0205131
Spatial Concept
5.

Rare soft tissue tumor

MedGen UID:
798555
Concept ID:
CN205605
Disease or Syndrome
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