Young-onset Parkinson disease (YOPD) is a form of Parkinson disease (PD), characterized by an age of onset between 21-45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints and falls, and other non-motor symptoms. A slow disease progression and a more pronounced response to dopaminergic therapy are also observed in most YOPD forms.
Synonyms: YOPD Early-onset Parkinson disease
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Term information
database cross reference
- OMIM:613643 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:600116 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:616840 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- ICD-10:G20 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- OMIM:300557 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- ICD-10:G20 (Attributed (The ICD10 code is attributed by Orphanet))
- OMIM:602404 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:606324 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:615528 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- OMIM:605909 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:610297 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:606852 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
hasDbXref
ICD-10:G20
OMIM:616840
OMIM:610297
OMIM:606852
OMIM:606324
OMIM:613643
OMIM:600116
OMIM:615528
OMIM:605909
OMIM:602404
OMIM:300557
Term relations
Subclass of:
- disease
- part_of some Primary orthostatic hypotension
- part_of some Genetic primary orthostatic hypotension
- has_inheritance some autosomal recessive
- has_inheritance some autosomal dominant
- present_in some Europe and has_point_prevalence_range some 1-5 / 10 000 and has_point_prevalence_average_value value 15.0
- present_in some Worldwide and has_point_prevalence_range some 1-5 / 10 000
- part_of some Rare parkinsonian syndrome due to neurodegenerative disease
- has_age_of_onset some adult
- part_of some Rare parkinsonian syndrome due to genetic neurodegenerative disease