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SMA2

disorder
SNOMED 128212001CUI C0393538

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormal electromyography finding
HP:0003457
Degeneration of alpha-motor neurons in anterior horn cells of the spinal cord
HP:0002398
Muscle atrophy, neurogenic
HP:0003202
Muscle weakness
HP:0001324
respiratory infections, recurrent
HP:0002205
Spinal muscle wasting
HP:0007269
Tongue fasciculations/fibrillations
HP:0001308
tremors in hands
HP:0002378

Quick Facts

SNOMED CT
128212001
UMLS CUI
C0393538
Fully Specified Name
Spinal muscular atrophy, type II (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
8
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.