Summary

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

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait