Disease #01487 (PEXPD (pain disorder, paroxysmal, extreme (PEXPD)), OMIM:167400)
| Official abbreviation |
PEXPD |
| Name |
pain disorder, paroxysmal, extreme (PEXPD) |
| OMIM ID |
167400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
SCN9A |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|