Diseases

Congenital hydronephrosis

congenital hydronephrosis

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Description: NCI2016_NCI-GLOSS_1602D:A type of bone cancer that usually starts in the lower spinal column or at the base of the skull.|NCI2016_CDISC_1602D:A malignant bone neoplasm arising from the remnants of the fetal notochord.|NCI2016_02D:A malignant bone tumor arising from the remnants of the fetal notochord. Although it can occur at all ages, it is more frequently seen in middle-aged adults. The most frequent sites of involvement are the sacrococcygeal area, spheno-occipital area, and cervico-thoraco-lumbar spine. Microscopically, chordomas are composed of cells that form cords and lobules, separated by mucoid intercellular tissue. Some of the cells are large (physaliphorous) and have vacuolated cytoplasm and prominent vesicular nuclei. Other tumor cells are small with small nuclei without visible nucleoli. Chordomas tend to recur and may metastasize. The most common sites of metastasis are the skin and bone.|MSH2017_2016_08_12:A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed)|HPO2016_07_04: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. [HPO:probinson]|CSP2006:malignant tumor arising from the embryonic remains of the notochord; also called chordocarcinoma, chordoepithelioma, and notochordoma.

Direct relations and traceable candidates grouped by relation type.

target disease8 Targets

aquaporin 1 (Colton blood group)

endothelin 1

epidermal growth factor