Vogt-koyanagi-harada Disease

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

Vogt-Koyanagi-Harada disease is a bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), auditory, and dermatological alterations.

Genes related to Vogt-koyanagi-harada Disease

FAS
IL23R
PTPN22
IFNA2

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Vogt-koyanagi-harada Disease

Short stature
Sensorineural hearing impairment
Cataract
Cognitive impairment
Visual impairment
Glaucoma
Retinal detachment
Sparse scalp hair
Hypopigmented skin patches
Premature graying of hair

And another 4 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Vogt-koyanagi-harada Disease Is also known as uveomenigitic syndrome.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Vogt-koyanagi-harada Disease Recommended genes panels

Panel Name, Specifity and genes Tested/covered
FAS Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). FAS Specificity 100 % Genes 25 %
Autoimmune Lymphoproliferative Syndrome Panel by next-generation sequencing (NGS). By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). FAS, FASLG, CASP10, CASP8, MAGT1, FADD, ITK, KRAS, NRAS Specificity 12 % Genes 25 %
Autoimmune Lymphoproliferative Syndrome Deletion/Duplication Panel. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). FAS, FASLG, CASP10, CASP8, MAGT1, FADD, ITK, KRAS, NRAS Specificity 12 % Genes 25 %
FAS Deletion/duplication analysis. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). FAS Specificity 100 % Genes 25 %
Tier 2: Hereditary Lymphoma and Immunodeficiency Panel. By Genetic Services Laboratory University of Chicago (United States). BLM, SH2D1A, BRCA1, BRCA2, STXBP2, FAS, CD27, FASLG, WAS, IKZF1, CASP10, CARD11, TNFRSF13B, ADA, DOCK8, CTLA4, MAGT1, ITK, NBN, NF1 , (...) View the complete list with 3 more genes Panel complete gene list BLM, SH2D1A, BRCA1, BRCA2, STXBP2, FAS, CD27, FASLG, WAS, IKZF1, CASP10, CARD11, TNFRSF13B, ADA, DOCK8, CTLA4, MAGT1, ITK, NBN, NF1, ATM, PIK3CD, PRF1 Specificity 5 % Genes 25 %
FAS (TNFRSF6) Gene Sequencing. By GeneDx (United States). FAS Specificity 100 % Genes 25 %
FAS. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). FAS Specificity 100 % Genes 25 %
Autoimmune lymphoproliferative syndrome (sequence analysis of FAS gene). By CGC Genetics (Portugal). FAS Specificity 100 % Genes 25 %

You can get up to 36 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

ORPHANET MESH Rare Disease Search Engine

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