Familial partial lipodystrophy associated with PLIN1 mutations (Q97021): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Refere-se a uma condição de pele autossômica dominante caracterizada pela perda de gordura subcutânea. Este diagnóstico é devido às mutações PLIN1.
@@ description / en / description / en @@
+This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is associated with PLIN1 mutations.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/98904071
@@ Property / Canonical URI: https://id.who.int/icd/entity/98904071 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_98904071
@@ Property / CURIE: CID11:ID_98904071 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_98904071
@@ Property / Canary Token: dki-india-ID_98904071 / 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 +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 13:03, 16 August 2026

This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is associated with PLIN1 mutations.

Language	Label	Description	Also known as
default for all languages	ID_98904071
English	Familial partial lipodystrophy associated with PLIN1 mutations	This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is associated with PLIN1 mutations.