Disease #01321 (erythromelalgia, primary, OMIM:133020)
Official abbreviation |
- |
Name |
erythromelalgia, primary |
OMIM ID |
133020 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
31 |
Phenotype entries for this disease |
31 |
Associated with 1 gene |
SCN9A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|