Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal nerve conduction study
Very frequent (80-99%)HP:0030177
Abnormality of vision
Very frequent (80-99%)HP:0000504
Axonal degeneration
Very frequent (80-99%)HP:0040078
Behavioral symptoms
Very frequent (80-99%)HP:0000708
Clumsiness
Very frequent (80-99%)HP:0002312
Distal muscle weakness in lower limbs
Very frequent (80-99%)HP:0009053
Fatty acids abnormal
Very frequent (80-99%)HP:0004359
Gait disturbance
Very frequent (80-99%)HP:0001288
Headache
Very frequent (80-99%)HP:0002315
Hyperactive behaviour
Very frequent (80-99%)HP:0000752
Impaired continence
Very frequent (80-99%)HP:0031064
Laboratory abnormality
Very frequent (80-99%)HP:0001939
Leg muscle stiffness
Very frequent (80-99%)HP:0008969
Loss of distal sensation
Very frequent (80-99%)HP:0002936
Mental-retardation
Very frequent (80-99%)HP:0001249
Partial paralysis of legs
Very frequent (80-99%)HP:0002385
Peripheral axonal degeneration
Very frequent (80-99%)HP:0000764
Poor vision
Very frequent (80-99%)HP:0000505
Progressive dementia
Very frequent (80-99%)HP:0000726
Progressive hearing loss
Very frequent (80-99%)HP:0001730
Progressive spastic paraparesis
Very frequent (80-99%)HP:0007199
Sensory impairment
Very frequent (80-99%)HP:0003474
Specific learning disability
Very frequent (80-99%)HP:0001328
Spinal cord disease
Very frequent (80-99%)HP:0002143
Visual loss
Very frequent (80-99%)HP:0000572
Abnormal erection
Frequent (30-79%)HP:0100639
Abnormal libido
Frequent (30-79%)HP:0031845
Abnormal skin colour
Frequent (30-79%)HP:0001000
Abnormality of adrenal physiology
Frequent (30-79%)HP:0011733
Adrenocortical abnormality
Frequent (30-79%)HP:0000849
Related Conditions
Neonatal adrenoleucodystrophy(child)
Adolescent X-linked adrenoleukodystrophy(child)
Childhood cerebral X-linked adrenoleukodystrophy(child)
AMN - adrenomyeloneuropathy(child)
Loss of single peroxisomal function(parent)
Hereditary disorder of endocrine system(parent)
Adrenal cortical hypofunction(parent)
Hereditary degenerative disease of central nervous system(parent)
Inherited metabolic disorder of nervous system(parent)
Leucodystrophy(parent)
X-linked hereditary disease(parent)
Quick Facts
- SNOMED CT
- 65389002
- UMLS CUI
- C0162309
- Fully Specified Name
- Adrenoleukodystrophy (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.