Disease #02331 (GLC3B (glaucoma, congenital, primary infantile, type 3B (GLC-3B)), OMIM:600975)
Official abbreviation |
GLC3B |
Name |
glaucoma, congenital, primary infantile, type 3B (GLC-3B) |
OMIM ID |
600975 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 2 genes |
CYP1B1, LTBP2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|