Disease Index

human disease

human disease

human disease

medical condition

congenital disorder of urinary system

medical condition

medical condition

amino acid metabolic disorder that involves a deficiency of one of the enzymes in the urea cycle which is responsible for removing ammonia from the blood stream

medical condition

Human disease

neoplasm involving the urinary system

medical condition

autosomal recessive disease that is characterized by inverted facial expressions in association with a severe and early-onset form of dysfunctional urinary voiding

human disease

most common form of cutaneous mastocytosis

skin condition

syndrome characterized by a combination of hearing loss and visual impairment

Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa

Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa

Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life

female reproductive organ cancer that is located in the uterus

uncommon malignant neoplasm arising from the uterine corpus. It is characterized by the presence of a malignant epithelial component and a benign mesenchymal (usually fibrous) component

Human disease

rare malignant heterologous neoplasm with skeletal muscle differentiation arising from the uterine corpus. It usually manifests with vaginal bleeding. The prognosis is poor

human disease

uterine corpus cancer that is located in the muscles of the uterus or located in other tissues that support the uterus

human disease

human disease

uterine Corpus sarcoma and leiomyosarcoma and uterine Corpus smooth muscle neoplasm that is located in the smooth muscle of the uterus