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cataract 13 with adult i phenotype

ORPHA: 91492

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

cataract that has material basis in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

Orphanet Code

ORPHA:91492
cataract 13 with adult i phenotype
OrphanetORPHA:91492
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO