Disease Index
9,486 diseasesvirginal breast hypertrophy
human disease
MeSH: C536821
visceral calciphylaxis
human disease
visceral heterotaxy
rare disease
MeSH: D059446
visceral leishmaniasis
human disease caused by protist parasites
ICD: B55.0MeSH: D007898
visceral malformation of the liver, biliary tract, pancreas or spleen
human disease
visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome
visual pathway glioma
human disease
visual snow syndrome
visual impairment
vitamin B12 deficiency anemia
disease
vitamin B12- and folate-independent constitutional megaloblastic anemia
human disease
vitamin B12-responsive methylmalonic acidemia
vitamin B12-responsive methylmalonic acidemia, type cblDv2
human disease
vitamin B12-unresponsive methylmalonic acidemia type mut-
vitamin B12-unresponsive methylmalonic acidemia type mut0
vitamin D-dependent rickets, type 2
a hereditary disorder of vitamin D action characterized by hypocalcemia, severe rickets and in many cases alopecia
vitelliform macular dystrophy
macular degeneration that can cause progressive vision loss, it is characterized by the disruption of cells in a small area near the center of the retina, the macula
MeSH: D057826
vitiligo
hypersensitivity reaction type II disease that causes depigmentation of skin patches resulting from loss of function or death of melanocytes
MeSH: D014820
vitiligo-associated multiple autoimmune disease susceptibility 1
human disease
vitreoretinal degeneration
human disease
vitreoretinopathy
group of diseases
Vogt–Koyanagi–Harada syndrome
multisystem disease
MeSH: D014607
Vohwinkel syndrome
human disease
ICD: Q82.8MeSH: C536457
von Economo's disease
atypical form of encephalitis
von Hippel anomaly
human disease
von Hippel-Lindau disease
a rare genetic disorder characterized by visceral cysts and benign tumors in multiple organ systems with potential for subsequent malignant change.
MeSH: D006623
von Voss-Cherstvoy syndrome
Von Voss-Cherstvoy syndrome is a very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities, and thrombocytopenia
MeSH: C565618
von willebrand disease type 2A
von willebrand disease type 2B
von willebrand disease type 2M
von willebrand disease type 2N