Phosphoserine Aminotransferase Deficiency, Infantile/juvenile Form

Phosphoserine Aminotransferase Deficiency, Infantile/juvenile Form(来自ICD-11)

别称:

Psat Deficiency, Infantile/juvenile Form

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Phosphoserine Aminotransferase Deficiency, Infantile/juvenile Form, is also known as psat deficiency, infantile/juvenile form. An important gene associated with Phosphoserine Aminotransferase Deficiency, Infantile/juvenile Form is PSAT1 (Phosphoserine Aminotransferase 1). Affiliated tissues include eye and skin, and related phenotypes are feeding difficulties in infancy and failure to thrive in infancy

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