A rare sex chromosome number anomaly disorder characterized, genetically, by the presence of an extra X and Y chromosome in males and, clinically, by tall stature, dysfunctional testes associated with infertility and insufficient testosterone production, cognitive, affective and social functioning impairments, global developmental delay, and an increased risk of congenital malformations.

This is just here as a test because I lose it

Term information

database cross reference
  • MedDRA:10048230 (E (Exact mapping: the two concepts are equivalent))
  • UMLS:C2936741 (E (Exact mapping: the two concepts are equivalent))
  • MeSH:D007713 (E (Exact mapping: the two concepts are equivalent))
  • ICD-10:Q98.8 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD10 code is attributed by Orphanet).)
expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=10

hasDbXref

MeSH:D007713

MedDRA:10048230

ICD-10:Q98.8

UMLS:C2936741

has age of onset

http://www.orpha.net/ORDO/Orphanet_409947

http://www.orpha.net/ORDO/Orphanet_409946

http://www.orpha.net/ORDO/Orphanet_409945

http://www.orpha.net/ORDO/Orphanet_409944

has birth prevalence range

http://www.orpha.net/ORDO/Orphanet_409977

has inheritance

http://www.orpha.net/ORDO/Orphanet_409939

http://www.orpha.net/ORDO/Orphanet_409941

has point prevalence range

http://www.orpha.net/ORDO/Orphanet_409981

notation

ORPHA:10

part of

http://www.orpha.net/ORDO/Orphanet_102283

http://www.orpha.net/ORDO/Orphanet_165707

http://www.orpha.net/ORDO/Orphanet_325546

http://www.orpha.net/ORDO/Orphanet_263749

http://www.orpha.net/ORDO/Orphanet_611327

present in

http://www.orpha.net/ORDO/Orphanet_409991

http://www.orpha.net/ORDO/Orphanet_409984

Term relations

Subclass of: