Uniparental disomies of paternal origin (Q46779): Difference between revisions

← Older edit

@@ Property / CURIE @@
+CID11:LD45.1
@@ Property / CURIE: CID11:LD45.1 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD45.1
@@ Property / Canary Token: dki-india-LD45.1 / 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 @@
+Q90-Q99
@@ Property / Linked ICD 10: Q90-Q99 / rank @@
+Normal rank

Latest revision as of 15:35, 13 August 2026

Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.

Language	Label	Description	Also known as
default for all languages	LD45.1
English	Uniparental disomies of paternal origin	Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.