Juvenile Huntington disease (JHD) is a form of Huntington disease (HD; see this term), characterized by onset of signs and symptoms before 20 years of age.

Synonyms:

Juvenile Huntington chorea

JHD

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Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=248111
hasDbXref
  • OMIM:143100
  • UMLS:C0751208
  • ICD-10:G10
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409946
  • http://www.orpha.net/ORDO/Orphanet_409947
has annual incidence range
  • http://www.orpha.net/ORDO/Orphanet_409979
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409976
notation
  • ORPHA:248111
part of
  • http://www.orpha.net/ORDO/Orphanet_306719
  • http://www.orpha.net/ORDO/Orphanet_519347
  • http://www.orpha.net/ORDO/Orphanet_276058
  • http://www.orpha.net/ORDO/Orphanet_98534
  • http://www.orpha.net/ORDO/Orphanet_522522
present in
  • http://www.orpha.net/ORDO/Orphanet_409984

Term relations