Familial benign copper deficiency (disorder)
SCTID: 763531001, Primitive, Active
763531001 |Familial benign copper deficiency (disorder)|
3642758018 - Familial benign copper deficiency (en) View
3642760016 - Familial benign copper deficiency (disorder) (en) View
3642761017 - Familial benign hypocupraemia (en) View
3642759014 - Familial benign hypocupremia (en) View
Relationship (9109134020) - 763531001 -> 32895009 (116680003) View
Relationship (15281261029) - 763531001 -> 1821000146108 (116680003) View
Relationship (9109133025) - 763531001 -> 19577007 (116680003) View
Relationship (9109135021) - 763531001 -> 79886009 (116680003) View
Relationship (9109136022) - 763531001 -> 111941005 (116680003) View
1821000146108 View
19577007 View
79886009 View
111941005 View
ExtendedMap object (29ae96e5-2a6d-5e25-8be5-df612f32c5d4) View
ExtendedMap object (98b7cbf9-1830-5e47-a825-972ab93e0b7f) View
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