Disease #01395 (ichthyosis vulgaris, OMIM:146700)
Official abbreviation |
- |
Name |
ichthyosis vulgaris |
OMIM ID |
146700 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
FLG |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2022-01-10 17:27:22 +01:00 (CET) |
Individuals
|