Disease #01311 (epidermolysis bullosa, pretibial, OMIM:131850)
Official abbreviation |
- |
Name |
epidermolysis bullosa, pretibial |
OMIM ID |
131850 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
6 |
Phenotype entries for this disease |
6 |
Associated with 1 gene |
COL7A1 |
Associated tissues |
- |
Disease features |
- |
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
|