| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities. (Human Disease Ontology, DOID_0060257) |
| External Link | http://www.omim.org/entry/127400 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the dyschromatosis symmetrica hereditaria phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ADAR | adenosine deaminase, RNA-specific |
