Copper Deficiency, Familial Benign

Copper Deficiency, Familial Benign(来自ICD-11)

别称:

Familial Benign Copper Deficiency

Familial Benign Hypocupremia

Copper Deficiency Familial Benign

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Copper Deficiency, Familial Benign, also known as familial benign copper deficiency, is related to hair morphology 2, and has symptoms including seizures Affiliated tissues include skin, and related phenotypes are abnormality of immune system physiology and decreased circulating copper concentration

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