cataract 3 multiple types
MeSH: C563294ORPHA: 217052
Overview
cataract that has material basis in heterozygous mutation in the beta-B2-crystallin gene (CRYBB2) on chromosome 22q11
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C563294Orphanet Code
ORPHA:217052cataract 3 multiple types
| MeSH | C563294 |
| Orphanet | ORPHA:217052 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO