Dyschromatosis Symmetrica Hereditaria, also known as dyschromatosis symmetrica hereditaria 1,is related to dyschromatosis universalis hereditaria 3 and aicardi-goutieres syndrome 6,and has symptoms including hypermelanotic macule, hypopigmented skin patches and hyperpigmented/hypopigmented macules. An important gene associated with Dyschromatosis Symmetrica Hereditaria is ADAR (Adenosine Deaminase, RNA Specific), and among its related pathways are C6 deamination of adenosine and Tyrosine metabolism. Affiliated tissues include skin and testes, and related mousephenotypes are hearing/vestibular/ear and neoplasm
Disease Interacts with Genes
Disease Interacts with Substances
Processes Associated With Trait
Molecular Function Associated With Trait
Biological Processes Associated With Trait
Pathways Associated With Trait
Symptoms Associated With Trait
Selected genes are highlighted in orange, bookmarked
genes are green
- Chemical increases gene,
- Chemical decreases gene,
- Chemical increases and decreases gene simultaneosly,
No arrows - gene doesn't interact with the chemical.
- Gene should be increased/decreased most of the time and the chemical does it.
- Gene should be increased/decreased most of the time but the chemical does the opposite.