Overview
Navajo neuropathy 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 balance
Always present (100%)HP:0002141
Absent Achilles reflex
Always present (100%)HP:0003438
Acute liver failure
Always present (100%)HP:0006554
Ankle weakness
Always present (100%)HP:0031374
Appendicular hypotonia
Always present (100%)HP:0012389
Bradycardia
Always present (100%)HP:0001662
Breakdown of light-sensitive cells in back of eye
Always present (100%)HP:0000556
Claw toe deformity
Always present (100%)HP:0034397
Decreased activity of mitochondrial complex III
Always present (100%)HP:0011924
Decreased number of large and small myelinated fibres
Always present (100%)HP:0003380
Dehydration
Always present (100%)HP:0001944
Depletion of mitochondrial DNA in liver
Always present (100%)HP:0006581
Depression
Always present (100%)HP:0000716
Dyschezia
Always present (100%)HP:0002019
Elevated alkaline phosphatase
Always present (100%)HP:0003155
Elevated brain lactate level by MRS
Always present (100%)HP:0012707
Elevated csf protein
Always present (100%)HP:0002922
EMG: myopathic changes
Always present (100%)HP:0003458
Eyelid ptosis
Always present (100%)HP:0000508
Fallen arches
Always present (100%)HP:0001763
Gait disturbance
Always present (100%)HP:0001288
Gallstones
Always present (100%)HP:0001081
Generalised decreased muscle tone
Always present (100%)HP:0001290
GI dysmotility
Always present (100%)HP:0002579
Global proximal tubulopathy
Always present (100%)HP:0012573
Hammertoe
Always present (100%)HP:0001765
Hearing impairment
Always present (100%)HP:0000365
High blood bilirubin levels
Always present (100%)HP:0002904
Hypertyrosinemia
Always present (100%)HP:0003231
Hyporeflexia at ankle joints
Always present (100%)HP:0009072
Related Conditions
Digestive system hereditary disorder(parent)
Recessive hereditary disorder (autosomal)(parent)
Depletion of mitochondrial DNA(parent)
Inherited metabolic disorder of nervous system(parent)
Metabolic and genetic disorder affecting the liver(parent)
Disorder of digestive system specific to fetus OR newborn(parent)
Quick Facts
- SNOMED CT
- 784346006
- UMLS CUI
- C1850406
- Fully Specified Name
- Navajo neurohepatopathy (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.