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
|