Parkinson Disease

Preferred Label : Parkinson Disease;

NCIt synonyms : Parkinson's Disease; Parkinson s Disease;

NCIt definition : A progressive degenerative disorder of the central nervous system characterized by loss of dopamine producing neurons in the substantia nigra and the presence of Lewy bodies in the substantia nigra and locus coeruleus. Signs and symptoms include tremor which is most pronounced during rest, muscle rigidity, slowing of the voluntary movements, a tendency to fall back, and a mask-like facial expression.;

Alternative definition : NCI-GLOSS: A progressive disorder of the nervous system marked by muscle tremors, muscle rigidity, decreased mobility, stooped posture, slow voluntary movements, and a mask-like facial expression.;

Codes from synonyms : CDR0000044140; G20;

Détails

Origin ID

C26845;

UMLS CUI

C0030567;

Automatic exact mappings (from CISMeF team)
- Parkinson disease [ACR pathology]
- Parkinson disease [OMIM phenotypic series]
- Parkinson's disease and parkinsonism [MedDRA High Level Term]
- Young onset Parkinson disease (disorder) [SNOMED CT concept]
- parkinson disease, secondary [MeSH Descriptor]
Currated CISMeF NLP mapping
- Disease Parkinson's [MedDRA LLT]
- Parkinson disease [PASCAL descriptor]
- Parkinson disease [Disease (Nov.)]
- Parkinson disease [ICD-11 Subcategory]
- Parkinson disease [Radlex concept]
- Parkinson disease [ORDO Disease]
- Parkinson's disease [LOINC component]
- Parkinson's disease [ICD-10 category]
- Parkinson's disease [DO Concept]
- Parkinson's disease [HPMULTI term]
- Parkinson's disease [ICD-9 code]
- Parkinson's disease [MedDRA Preferred Term]
- Parkinson's disease NOS [MedDRA LLT]
- Parkinsons disease [ICD-10 category (who)]
- parkinson disease [MeSH Descriptor]
- parkinson disease [MeSH concept]
- parkinson's disease [MedlinePlus Topic]
- parkinson's disease, nos [SNOMED Notion]
- parkinsonian disorders [MeSH Descriptor]
- parkinsonism [ICPC-2 Rubric]
DO Cross reference
- Parkinson's disease [DO Concept]
False automatic mappings
- Parkinson's disease (disorder) [SNOMED CT concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disease Parkinson's [MedDRA LLT]
- PARALYSIS AGITANS [WHO-ART Included Term]
- Paralysis agitans [ICD-9 code]
- Paralysis agitans [MedDRA LLT]
- Parkinson disease [ORDO Disease]
- Parkinson disease [Radlex concept]
- Parkinson disease [PASCAL descriptor]
- Parkinson disease [Disease (Nov.)]
- Parkinson disease [ICD-11 Subcategory]
- Parkinson's disease [MedDRA Preferred Term]
- Parkinson's disease [LOINC component]
- Parkinson's disease [ICD-10 category]
- Parkinson's disease [DO Concept]
- Parkinson's disease [ICD-9 code]
- Parkinson's disease (disorder) [SNOMED CT concept]
- Parkinson's disease NOS [MedDRA LLT]
- Parkinson's syndrome [MedDRA LLT]
- Parkinsonism [ICD-11 Category]
- Parkinsons disease [ICD-10 category (who)]
- parkinson disease [MeSH Descriptor]
- parkinson disease [MeSH concept]
- parkinson's disease [MedlinePlus Topic]
- parkinson's disease, nos [SNOMED Notion]
associated_with_malfunction_of_gene_product
- Alpha-Synuclein [NCIt concept]
- E3 Ubiquitin-Protein Ligase Parkin [NCIt concept]
- Leucine-Rich Repeat Serine/Threonine-Protein Kinase 2 [NCIt concept]
concept_is_in_subset
- CPTAC Causes of Death Codelist [NCIt concept]
- CPTAC Codelists Terminology [NCIt concept]
- CPTAC Medical Conditions Codelist [NCIt concept]
- CPTAC Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- mCode Elixhauser Neurological Movement Disorder Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_associated_gene
- LRRK2 Gene [NCIt concept]
- LRRK2 wt Allele [NCIt concept]
- MIR133B Gene [NCIt concept]
- MIR133B wt Allele [NCIt concept]
- MIR433 Gene [NCIt concept]
- MIR433 wt Allele [NCIt concept]
- NOS1 Gene [NCIt concept]
- NOS1 wt Allele [NCIt concept]
- PRKN Gene [NCIt concept]
- PRKN wt Allele [NCIt concept]
- SNCA Gene [NCIt concept]
- SNCA wt Allele [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]

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