Disease Index

von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material basis in heterozygous mutation in the VWF gene on chromosome 12p13

von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has material basis in mutation in the VWF gene which maps to chromosome 12p13

human disease

vulva carcinoma that derives from epithelial cells of glandular origin

Human disease

vulva cancer that has material basis in abnormally proliferating cells derives from epithelial cells

vulva carcinoma and has material basis in squamous cells and is located in the epidermis of the vulvar tissue

Intraepithelial neoplasia of the vulvar squamous epithelium. There is no evidence of invasion. This category includes vulvar high grade squamous intraepithelial lesion and vulvar intraepithelial neoplasia, differentiated type.

human disease

rare hereditary syndrome

human disease

human disease

Waardenburg-Shah syndrome (WSS) is a neurocristopathy characterized by the association of Waardenburg syndrome (sensorineural hearing loss and pigmentary abnormalities; see this term) and Hirschsprung disease (see this term)

genetic condition involving hearing loss and depigmentation

human disease

Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment

rare genetic syndrome in which affected children are predisposed to develop Wilms tumour

Type of blood cancer

medical condition

rare form of autosomal recessive congenital muscular dystrophy

medical condition

autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism

Disorder of the embryo caused by maternal warfarin administration

form of autoimmune hemolytic anemia

Human disease

rare, usually solitary, benign epithelial tumor of the skin that appears to arise from a hair follicle. It usually develops in the head and neck region as a nodular lesion with a central keratotic plug

adrenal gland disease that is characterized by failure of the adrenal gland due to bleeding into the gland

medical condition

human disease