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Vogt-Koyanagi-Harada

Disease information

Vogt-Koyanagi-Harada (VKH) is a multisystem disease having autoimmune causes that affect melanin-pigmented tissues, sometimes called Harada syndrome or uveomeningitis syndrome. The most noticeable symptom is a rapid loss of vision, which may also manifest neurological signs, loss of hearing, loss of hair, and ski color changes. Its sequence of symptoms and manifestations can be divided into four phases - prodromal, acute uveitic, convalescent, and chronic recurrent. Some may be caused by a viral infection, but the exact causes are not known yet.

Wikipedia - Vogt-Koyanagi-Harada

NORD - National Organization for Rare Disorders

Demographics

Total samples: 83
Females: 17
Males: 49
Age: 38.3 (13-77)
BMI: 22.8 (15.4-33.0)

Species association

Enriched in 5 species
Depleted in 12 species

Cohorts

hgma409 - VKH - China

Bioprojects included

PRJNA356225 - 10.1080/19490976.2019.1700754

Relative abundance

Phylum
Family
Genus

Richness overview

Gene

Species

Richness overview (per cohort)

Gene

Species