Disease #01235 (CTRCT1 (cataract, type 1 (CTRCT1)), OMIM:116200)
Official abbreviation |
CTRCT1 |
Name |
cataract, type 1 (CTRCT1) |
OMIM ID |
116200 |
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 |
GJA8 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-11-20 17:38:33 +01:00 (CET) |
Individuals
|
|