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
- ICD-10:G10 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD code is attributed by Orphanet).)
- OMIM:143100 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- UMLS:C0751208 (E (Exact mapping: the two concepts are equivalent))
definition citation
- Orphanet
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
Subclass of:
Related from: