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Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

disorder
SNOMED 733599009CUI C4518838

Overview

Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency 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.

Adult onset sensorineural hearing impairment
Frequent (30-79%)HP:0008615
Bilateral ptosis
Frequent (30-79%)HP:0001488
Deglutition disorder
Frequent (30-79%)HP:0002015
External ophthalmoplegia, progressive
Frequent (30-79%)HP:0000590
Limb-girdle muscle weakness
Frequent (30-79%)HP:0003325
Limb-girdle myopathy
Frequent (30-79%)HP:0003797
Lower limb muscle weakness
Frequent (30-79%)HP:0007340
Peripheral sensory axonal neuropathy
Frequent (30-79%)HP:0003390
Ataxia
Occasional (5-29%)HP:0001251
Cataract
Occasional (5-29%)HP:0000518
Cognitive deficits
Occasional (5-29%)HP:0100543
Depression
Occasional (5-29%)HP:0000716
Dysphonia
Occasional (5-29%)HP:0001618
Hip-girdle muscle weakness
Occasional (5-29%)HP:0003749
Muscle pain
Occasional (5-29%)HP:0003326
Muscle spasm
Occasional (5-29%)HP:0003394
Optic atrophy
Occasional (5-29%)HP:0000648
Progressive dementia
Occasional (5-29%)HP:0000726
Prostration
Occasional (5-29%)HP:0025406
Squint
Occasional (5-29%)HP:0000486
Viral infection-induced rhabdomyolysis
Occasional (5-29%)HP:0003558

Quick Facts

SNOMED CT
733599009
UMLS CUI
C4518838
Fully Specified Name
Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
21
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.