Disease #01282 (Dermatopathia pigmentosa reticularis, OMIM:125595)
Official abbreviation |
- |
Name |
Dermatopathia pigmentosa reticularis |
OMIM ID |
125595 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
KRT14 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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