Disease #06812 (GLC3E (Glaucoma 3, primary congenital, E), OMIM:617272)
Official abbreviation |
GLC3E |
Name |
Glaucoma 3, primary congenital, E |
OMIM ID |
617272 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
6 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TEK |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|