Immunodeficiency with factor D anomaly (Q39708): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A deficiência de fator D é um transtorno imunológico autossômico recessivo caracterizado por suscetibilidade aumentada a infecções bacterianas, particularmente infecções por Neisseria, devido a um defeito na via alternativa do complemento.
@@ description / en / description / en @@
+Factor D deficiency is an autosomal recessive immunologic disorder characterised by increased susceptibility to bacterial infections, particularly Neisseria infections, due to a defect in the alternative complement pathway.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1998425794
@@ Property / Canonical URI: https://id.who.int/icd/entity/1998425794 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:4A00.13
@@ Property / CURIE: CID11:4A00.13 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-4A00.13
@@ Property / Canary Token: dki-india-4A00.13 / 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
@@ Property / Linked ICD 10 @@
+D84.1
@@ Property / Linked ICD 10: D84.1 / rank @@
+Normal rank

Latest revision as of 05:13, 13 August 2026

Factor D deficiency is an autosomal recessive immunologic disorder characterised by increased susceptibility to bacterial infections, particularly Neisseria infections, due to a defect in the alternative complement pathway.

Language	Label	Description	Also known as
default for all languages	4A00.13
English	Immunodeficiency with factor D anomaly	Factor D deficiency is an autosomal recessive immunologic disorder characterised by increased susceptibility to bacterial infections, particularly Neisseria infections, due to a defect in the alternative complement pathway.