46,XX disorders of sex development (Q54946913): Difference between revisions

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‎Removed claim: UMLS CUI (P2892): C0238394
Tag: Wikidata user interface
‎Removed claim: UMLS CUI (P2892): C0238394
Tag: Wikidata user interface
Property / UMLS CUI
 
Property / UMLS CUI: C0238394 / rank
Normal rank
 
Property / UMLS CUI: C0238394 / reference
stated in: Human Phenotype Ontology release 2018-03-08
retrieved: 8 October 2018
Timestamp+2018-10-08T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Human Phenotype Ontology ID: HP:0010458
 

Revision as of 02:23, 30 November 2022

congenital conditions in individuals with a female karyotype, in which the development of the gonadal or anatomical sex is atypical
  • 46,XX Differences of Sex Development
  • 46,XX Disorders of Sex Development
  • 46,XX DSD
  • female pseudohermaphroditism
Language Label Description Also known as
English
46,XX disorders of sex development
congenital conditions in individuals with a female karyotype, in which the development of the gonadal or anatomical sex is atypical
  • 46,XX Differences of Sex Development
  • 46,XX Disorders of Sex Development
  • 46,XX DSD
  • female pseudohermaphroditism

Statements

subclass of
disease
0 references

Identifiers

MeSH tree code
C12.706.316.064
0 references
C13.351.875.253.064
0 references
C16.131.939.316.064
0 references
C19.391.119.064
0 references
 
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