All diseases

OMIM ID
309400
OMIM term:
MENKES DISEASE
Alternative terms:
MK; MNK
MENKES SYNDROME
KINKY HAIR DISEASE
STEELY HAIR DISEASE
COPPER TRANSPORT DISEASE
(∗) Location:
Xq21.1  
(†) Associated OMIM genes:
ATP7A  
(‡) Associated MGI genes:
Atp7a   Lox  

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* quick link - http://q.sanger.ac.uk/yudpp8f7