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Galactosemia (Hepatic Form) — Gene Therapy & Clinical Trials | FollowGene

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Home/Diseases/Galactosemia (Hepatic Form)

Galactosemia (Hepatic Form)

Prevalence: 1/50000

hepatic

Official·OMIM:230400 Official·ORPHA79239

Neonatal liver failure due to GALT gene mutations.

Associated Genes

No gene records found associated with this disease.

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