[genetically determined biochemical disorders in metal absorption, metal excretion, metal transport, or incorporation of metal to protein or enzyme. ( CSP )]
UMLS (CSP) C0025534 Relation/PAR: Congenital Metabolic 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