Disease #00075 (CA (congenital aniridia), OMIM:106210)
Official abbreviation |
CA |
Name |
congenital aniridia |
OMIM ID |
106210 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PAX6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|