Overview
Infantile striatonigral degeneration 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.
Choreoathetoid movements
HP:0001266
Deglutition disorder
HP:0002015
Developmental stagnation
HP:0007281
Dystonic disease
HP:0001332
Involuntary muscle stiffness, contraction, or spasm
HP:0001257
Mental deficiency
HP:0001249
Nystagmus, pendular
HP:0012043
Optic atrophy
HP:0000648
Postnatal failure to thrive
HP:0001508
Psychomotor regression
HP:0002376
Quick Facts
- SNOMED CT
- 718174008
- UMLS CUI
- C0795996
- Fully Specified Name
- Infantile striatonigral degeneration (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 10
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.