JUV EPITH CORNEA DYSTRPH

[An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder. ( MSH )]

UMLS (ICD9CM) C0339277

Congenital Abnormality

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