Autosomal dominant late onset Parkinson disease

disorder

SNOMED 716662004CUI C4274355

Overview

Autosomal dominant late onset Parkinson disease is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Parkinsonian disease

Always present (100%)HP:0001300

Akinesia

Frequent (30-79%)HP:0002304

Chronic constipation

Frequent (30-79%)HP:0012450

Deglutition disorder

Frequent (30-79%)HP:0002015

Double vision

Frequent (30-79%)HP:0000651

Frequent falls

Frequent (30-79%)HP:0002359

Parkinsonism with favorable response to dopaminergic medication

Frequent (30-79%)HP:0002548

Sense of smell impaired

Frequent (30-79%)HP:0004409

Spastic/hyperactive bladder

Frequent (30-79%)HP:0005340

Tremor at rest

Frequent (30-79%)HP:0002322

Cerebral cortex atrophy

Occasional (5-29%)HP:0002120

Depressive episode

Occasional (5-29%)HP:0000716

Dyskinesia

Occasional (5-29%)HP:0100660

Dystonic disease

Occasional (5-29%)HP:0001332

Excess astrocytes in brain

Occasional (5-29%)HP:0002171

Flat speech

Occasional (5-29%)HP:0031435

Hypomimic face

Occasional (5-29%)HP:0000338

Imbalance

Occasional (5-29%)HP:0002172

Impulsivity

Occasional (5-29%)HP:0100710

Intellectual deterioration

Occasional (5-29%)HP:0001268

Intolerance to frustration

Occasional (5-29%)HP:0000744

Lack of feeling, emotion, interest

Occasional (5-29%)HP:0000741

Lewy bodies

Occasional (5-29%)HP:0100315

Muscle rigidity

Occasional (5-29%)HP:0002063

Muscle spasm

Occasional (5-29%)HP:0003394

Orthostatic hypotension due to autonomic dysfunction

Occasional (5-29%)HP:0004926

Psychomotor agitation

Occasional (5-29%)HP:0000713

Shuffled walk

Occasional (5-29%)HP:0002362

Slowness of movements

Occasional (5-29%)HP:0002067

Trouble sleeping

Occasional (5-29%)HP:0002360

Related Conditions

Autosomal dominant hereditary disorder(parent)

Parkinson's disease(parent)

Hereditary degenerative disease of central nervous system(parent)

Quick Facts

SNOMED CT: 716662004
UMLS CUI: C4274355
Fully Specified Name: Autosomal dominant late onset Parkinson disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.