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inborn metal metabolism disorder
[genetically determined biochemical disorders in metal absorption, metal excretion, metal transport, or incorporation of metal to protein or enzyme. ( CSP )]
UMLS (CSP) C0025534- Disease or Syndrome
Relation/PAR: Congenital Metabolic Disorder
metal metabolism disorder
metal metabolism disorder
Relation/CHD: cerebral pseudosclerosis
kinky hair syndrome
familial periodic paralysis
hereditary hemochromatosis
diabetes bronze
cerebral pseudosclerosis
hypophosphatasia
Hypophosphatemia, Familial
kinky hair syndrome
familial periodic paralysis
Albright's hereditary osteodystrophy
kinky hair syndrome
familial periodic paralysis
hereditary hemochromatosis
diabetes bronze
cerebral pseudosclerosis
hypophosphatasia
Hypophosphatemia, Familial
kinky hair syndrome
familial periodic paralysis
Albright's hereditary osteodystrophy
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