Autosomal dominant striatal neurodegeneration

disorder

SNOMED 725392005CUI C4511004

Overview

Autosomal dominant striatal neurodegeneration 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.

Abnormality of movement

Very frequent (80-99%)HP:0100022

Difficulty articulating speech

Very frequent (80-99%)HP:0001260

Dysdiadochokinesis

Very frequent (80-99%)HP:0002075

Muscle rigidity

Very frequent (80-99%)HP:0002063

Slowness of movements

Very frequent (80-99%)HP:0002067

Deglutition disorder

Frequent (30-79%)HP:0002015

Gait disturbance

Frequent (30-79%)HP:0001288

Related Conditions

Autosomal dominant hereditary disorder(parent)

Parkinsonism(parent)

Cerebral degeneration(parent)

Hereditary degenerative disease of central nervous system(parent)

Abnormal corpus striatum morphology(parent)

Quick Facts

SNOMED CT: 725392005
UMLS CUI: C4511004
Fully Specified Name: Autosomal dominant striatal neurodegeneration (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.