Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 763531001

Production
The component that hold information about this concept.
Familial benign copper deficiency (disorder)
Familial benign hypocupremia
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Familial benign copper deficiency (disorder)

SCTID: 763531001, Primitive, Active


763531001|Familial benign copper deficiency (disorder)|
  • en Familial benign copper deficiency
  • en Familial benign copper deficiency (disorder)
  • en Familial benign hypocupraemia
  • en Familial benign hypocupremia

763531001 |Familial benign copper deficiency (disorder)|

<<< 19577007 |Hypocupremia (disorder)| +
    79886009 |Disorder of copper metabolism (disorder)| +
    111941005 |Familial disease (disorder)| +
    1821000146108 |Hereditary metabolic disease (disorder)|
Active
esc