16 Parents
Identifier | Name | Description |
---|---|---|
DOID:0050686 | organ system cancer | A cancer that is classified based on the organ it starts in. |
DOID:162 | cancer | A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis. |
DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
DOID:14566 | disease of cellular proliferation | A disease that is characterized by abnormally rapid cell division. |
DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
DOID:17 | musculoskeletal system disease | A disease of anatomical entity that occurs in the muscular and/or skeletal system. |
DOID:0080001 | bone disease | A connective tissue disease that affects the structure or development of bone or causes an impairment of normal bone function. |
DOID:65 | connective tissue disease | A musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage. |
DOID:201 | connective tissue cancer | A musculoskeletal system cancer that is located_in connective tissue. |
DOID:0060100 | musculoskeletal system cancer | An organ system cancer located_in the muscular and skeletal organs and characterized by uncontrolled cellular proliferation of the musculoskeletal organs. |
DOID:184 | bone cancer | A connective tissue cancer that is located_in bone and is characterized by uncontrolled cellular proliferation that destroys normal bone tissue. |
DOID:0080639 | bone sarcoma | A bone cancer that has_material_basis_in abnormally proliferating cells derives from embryonic mesoderm. |
DOID:3347 | osteosarcoma | A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. It usually involves bones and less frequently extraosseous sites. It often involves the long bones (particularly distal femur, proximal tibia, and proximal humerus). |
DOID:3376 | bone osteosarcoma | An osteosarcoma that is an usually aggressive malignant bone-forming mesenchymal neoplasm arising from the bone. It may arise de novo or from a pre-existing lesion of the bone. Pain and a palpable mass are the most frequent clinical sign and symptom. It may spread to other anatomic sites, particularly the lungs. |
DOID:7602 | conventional osteosarcoma | A bone osteosarcoma that is characterized by the presence of osteoid extracellular matrix and that arises from the medullary portion of the bone. It affects the long bones and most commonly, the distal femur, proximal tibia, and proximal humerus. Pain with or without a palpable mass is the most common clinical presentation. |
DOID:6951 | telangiectatic osteogenic sarcoma |
15 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:7602 | DOID:6951 |
is_a | DOID:4 | DOID:6951 |
is_a | DOID:0060100 | DOID:6951 |
is_a | DOID:14566 | DOID:6951 |
is_a | DOID:17 | DOID:6951 |
is_a | DOID:7 | DOID:6951 |
is_a | DOID:201 | DOID:6951 |
is_a | DOID:0080001 | DOID:6951 |
is_a | DOID:65 | DOID:6951 |
is_a | DOID:0080639 | DOID:6951 |
is_a | DOID:0050686 | DOID:6951 |
is_a | DOID:3376 | DOID:6951 |
is_a | DOID:3347 | DOID:6951 |
is_a | DOID:184 | DOID:6951 |
is_a | DOID:162 | DOID:6951 |