Male with 46,XX karyotype (Q46771): Difference between revisions

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@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/594136490
@@ Property / Canonical URI: https://id.who.int/icd/entity/594136490 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD52.0
@@ Property / CURIE: CID11:LD52.0 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD52.0
@@ Property / Canary Token: dki-india-LD52.0 / 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 15:34, 13 August 2026

A disease affecting males, characterised by hypergonadotropic hypogonadism, testosterone deficiency, and infertility. This condition may also present with hypospadias. This disease may be associated with abnormal crossing over of the sex chromosomes during meiosis in the father, resulting in the SRY gene being present on one or both copies of the X chromosome.

Language	Label	Description	Also known as
default for all languages	LD52.0
English	Male with 46,XX karyotype	A disease affecting males, characterised by hypergonadotropic hypogonadism, testosterone deficiency, and infertility. This condition may also present with hypospadias. This disease may be associated with abnormal crossing over of the sex chromosomes during meiosis in the father, resulting in the SRY gene being present on one or both copies of the X chromosome.