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bn:00248251n
Noun Concept
SYL
No term available
EN
Menkes disease, also known as Menkes syndrome, is an X-linked recessive disorder caused by mutations in genes coding for the copper-transport protein ATP7A, leading to copper deficiency. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
metal metabolism disorder
GENETIC ASSOCIATION
EN
ATP7A
HEALTH SPECIALTY
EN
endocrinology

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