Congenital Cataract-Severe Neonatal Hepatopathy-Global Developmental Delay Syndrome

Congenital Cataract-Severe Neonatal Hepatopathy-Global Developmental Delay Syndrome(来自ICD-11)

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Congenital Cataract-Severe Neonatal Hepatopathy-Global Developmental Delay Syndrome An important gene associated with Congenital Cataract-Severe Neonatal Hepatopathy-Global Developmental Delay Syndrome is CYP51A1 (Cytochrome P450 Family 51 Subfamily A Member 1). Affiliated tissues include liver and eye.

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