Disease #05568 (KCTN1 (keratoconus, type 1 (KTCN-1)), OMIM:148300)
| Official abbreviation |
KCTN1 |
| Name |
keratoconus, type 1 (KTCN-1) |
| OMIM ID |
148300 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
VSX1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2019-02-14 12:42:52 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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