Disease #02873 (CTRCT22;CATCN2 (cataract, type 22 (CTRCT-22, cataract congenital nuclear, autosomal recessive 2 CATCN-2))), OMIM:609741)
| Official abbreviation |
CTRCT22;CATCN2 |
| Name |
cataract, type 22 (CTRCT-22, cataract congenital nuclear, autosomal recessive 2 CATCN-2)) |
| OMIM ID |
609741 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CRYBB3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
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