Mosaicism, 45, X or other cell line with abnormal sex chromosome (Q46916): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Doença causada por fusão embrionária ou mutação estrutural de um cromossomo sexual no início do desenvolvimento embrionário, resultando em um subconjunto de células no corpo com uma cópia normal do cromossomo X e um cromossomo sexual anormal. Esta doença pode se apresentar com baixa estatura, disfunção dos órgãos sexuais ou pode ser assintomática.
@@ description / en / description / en @@
+A disease caused by embryonic fusion or the structural mutation of a sex chromosome early in embryonic development, resulting in a subset of cells in the body having one normal copy of the X chromosome and one abnormal sex chromosome. This disease may present with short stature, sexual organ dysfunction, or may be asymptomatic.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/50021633
@@ Property / Canonical URI: https://id.who.int/icd/entity/50021633 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD50.04
@@ Property / CURIE: CID11:LD50.04 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD50.04
@@ Property / Canary Token: dki-india-LD50.04 / 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 @@
+Q96.4
@@ Property / Linked ICD 10: Q96.4 / rank @@
+Normal rank

Latest revision as of 15:48, 13 August 2026

A disease caused by embryonic fusion or the structural mutation of a sex chromosome early in embryonic development, resulting in a subset of cells in the body having one normal copy of the X chromosome and one abnormal sex chromosome. This disease may present with short stature, sexual organ dysfunction, or may be asymptomatic.

Language	Label	Description	Also known as
default for all languages	LD50.04
English	Mosaicism, 45, X or other cell line with abnormal sex chromosome	A disease caused by embryonic fusion or the structural mutation of a sex chromosome early in embryonic development, resulting in a subset of cells in the body having one normal copy of the X chromosome and one abnormal sex chromosome. This disease may present with short stature, sexual organ dysfunction, or may be asymptomatic.