MedGen

A disorder that results from a chromosomal abnormality. [from NCI]

A chromosomal abnormality in which there is an addition or loss of chromosomes within a set (e.g., 23 + 22 or 23 + 24). [from NCI]

A cancer of the prostate. [from HPO]

A carcinoma that arises from the prostate gland and has spread to other anatomic sites. [from NCI]

The presence of inflammation of the prostate. [from HPO]

A rare developmental defect during embryogenesis characterized by multifocal dilated lymphatic vessels involving multiple organs and tissues. Patients mostly present in infancy and childhood. Clinical course and prognosis depend on the affected sites and extent of the condition, deterioration of lung function being a major cause of morbidity and mortality. [from ORDO]

A neoplastic process that affects the squamous epithelium of the cervix. It is classified as cervical squamous intraepithelial neoplasia 1, 2, or 3, according to the degree of squamous cell maturation and cellular atypia, and the number of mitotic figures. [from NCI]

A neoplasm that affects the male reproductive system. [from HPO]

A benign, borderline, or malignant neoplasm that affects the prostate gland. Representative examples include benign prostate phyllodes tumor, prostatic intraepithelial neoplasia, prostate carcinoma, and prostate sarcoma. [from NCI]

A non-neoplastic or neoplastic disorder that affects the prostate gland. Representative examples include prostatitis, prostatic intraepithelial neoplasia, and carcinoma. [from NCI]