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: JHD Juvenile Huntington chorea
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Term information
database cross reference
- OMIM:143100 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- ICD-10:G10 (Attributed (The ICD10 code is attributed by Orphanet))
- UMLS:C0751208 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:G10 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
Term relations
Subclass of:
- disease
- part_of some Neurodegenerative disease with chorea
- part_of some Rare genetic neuromuscular disorder with ocular motility/alignment anomaly
- part_of some Rare neuromuscular disorder with ocular motility/alignment anomaly
- has_annual_incidence_range some <1 / 1 000 000 and present_in some Europe and has_annual_incidence_average_value value 0.04
- has_age_of_onset some adolescent
- part_of some Genetic neurodegenerative disease with dementia
- has_inheritance some autosomal dominant
- has_age_of_onset some childhood
- present_in some Europe and has_point_prevalence_range some 1-9 / 1 000 000 and has_point_prevalence_average_value value 0.6
- part_of some Neurodegenerative disease with dementia
- part_of some Genetic neurodegenerative disease
Related from: