Benign familial copper deficiency (Q83523): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Trata-se de transtorno hematológico e neurológico familiar benigno muito raro. A doença envolve uma deficiência nutricional do oligoelemento cobre. O cobre é onipresente e a necessidade diária é baixa, tornando a deficiência de cobre adquirida muito rara. A deficiência de cobre pode se manifestar em paralelo com a vitamina B12 e outras deficiências nutricionais.
@@ description / en / description / en @@
+This is a benign familial very rare haematological and neurological disorder. The disease involves a nutritional deficiency in the trace element copper. Copper is ubiquitous and daily requirement is low making acquired copper deficiency very rare. Copper deficiency can manifest in parallel with vitamin B12 and other nutritional deficiencies .
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/580108812
@@ Property / Canonical URI: https://id.who.int/icd/entity/580108812 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_580108812
@@ Property / CURIE: CID11:ID_580108812 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_580108812
@@ Property / Canary Token: dki-india-ID_580108812 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest revision as of 08:53, 15 August 2026

This is a benign familial very rare haematological and neurological disorder. The disease involves a nutritional deficiency in the trace element copper. Copper is ubiquitous and daily requirement is low making acquired copper deficiency very rare. Copper deficiency can manifest in parallel with vitamin B12 and other nutritional deficiencies .

Language	Label	Description	Also known as
default for all languages	ID_580108812
English	Benign familial copper deficiency	This is a benign familial very rare haematological and neurological disorder. The disease involves a nutritional deficiency in the trace element copper. Copper is ubiquitous and daily requirement is low making acquired copper deficiency very rare. Copper deficiency can manifest in parallel with vitamin B12 and other nutritional deficiencies .