Adrenoleukodystrophy

UMLS: C0162309
Basic Information
Severity Level:
Critical
Based on 5 similar ADEs (max similarity: 0.599)
Definition:
An X-linked recessive disorder characterized by the accumulation of saturated very long chain fatty acids in the LYSOSOMES of ADRENAL CORTEX and the white matter of CENTRAL NERVOUS SYSTEM. This disease occurs almost exclusively in the males. Clinical features include the childhood onset of ATAXIA; NEUROBEHAVIORAL MANIFESTATIONS; HYPERPIGMENTATION; ADRENAL INSUFFICIENCY; SEIZURES; MUSCLE SPASTICITY; and DEMENTIA. The slowly progressive adult form is called adrenomyeloneuropathy. The defective gene ABCD1 is located at Xq28, and encodes the adrenoleukodystrophy protein (ATP-BINDING CASSETTE TRANSPORTERS).
UMLS ID:
C0162309
MeSH ID:
Synonyms:
Adrenoleukodystrophy
Ald
Ald - Adrenoleukodystrophy
Addison Disease-Cerebral Sclerosis Syndrome
Addison Disease-Spastic Paraplegia Syndrome
Addison-Schilder Disease
Addison-Schilder Syndrome
Addison-Schilder; Complex
Adrenoleukodystrophy
Bronze Schilder Disease
Fanconi-Prader Syndrome
Schilder Disease
Schilder-Addison Complex
Schilder-Addison; Complex
Classification Hierarchy
MeSH Tree Number breakdown for C0162309
C10
Nervous System Diseases
Category: Nervous System Diseases Parent: C (Diseases) Level: 0
C10.228
Central Nervous System Diseases
Category: Nervous System Diseases Parent: C10 Level: 1
C10.228.140
Brain Diseases
Category: Nervous System Diseases Parent: C10.228 Level: 2
C10.228.140.163
Brain Diseases, Metabolic
Category: Nervous System Diseases Parent: C10.228.140 Level: 3
C10.228.140.163.100
Brain Diseases, Metabolic, Inborn
Category: Nervous System Diseases Parent: C10.228.140.163 Level: 3
C10.228.140.163.100.084
Adrenoleukodystrophy
Category: Nervous System Diseases Parent: C10.228.140.163.100 Level: 4 Tree Number: C10.228.140.163.100.084
C10
Nervous System Diseases
Category: Nervous System Diseases Parent: C (Diseases) Level: 0
C10.228
Central Nervous System Diseases
Category: Nervous System Diseases Parent: C10 Level: 1
C10.228.140
Brain Diseases
Category: Nervous System Diseases Parent: C10.228 Level: 2
C10.228.140.163
Brain Diseases, Metabolic
Category: Nervous System Diseases Parent: C10.228.140 Level: 3
C10.228.140.163.100
Brain Diseases, Metabolic, Inborn
Category: Nervous System Diseases Parent: C10.228.140.163 Level: 3
C10.228.140.163.100.362
Hereditary Central Nervous System Demyelinating Diseases
Category: Nervous System Diseases Parent: C10.228.140.163.100 Level: 4 Tree Number: C10.228.140.163.100.362
C10
Nervous System Diseases
Category: Nervous System Diseases Parent: C (Diseases) Level: 0
C10.228
Central Nervous System Diseases
Category: Nervous System Diseases Parent: C10 Level: 1
C10.228.140
Brain Diseases
Category: Nervous System Diseases Parent: C10.228 Level: 2
C10.228.140.695
Leukoencephalopathies
Category: Nervous System Diseases Parent: C10.228.140 Level: 3 Tree Number: C10.228.140.695
C10
Nervous System Diseases
Category: Nervous System Diseases Parent: C (Diseases) Level: 0
C10.314
Demyelinating Diseases
Category: Nervous System Diseases Parent: C10 Level: 1
C10.314.400
Hereditary Central Nervous System Demyelinating Diseases
Category: Nervous System Diseases Parent: C10.314 Level: 2
C10.314.400.250
Adrenoleukodystrophy
Category: Nervous System Diseases Parent: C10.314.400 Level: 3 Tree Number: C10.314.400.250
C10
Nervous System Diseases
Category: Nervous System Diseases Parent: C (Diseases) Level: 0
C10.597
Neurologic Manifestations
Category: Nervous System Diseases Parent: C10 Level: 1 Tree Number: C10.597
C16
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C (Diseases) Level: 0
C16.320
Genetic Diseases, Inborn
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16 Level: 1
C16.320.322
Genetic Diseases, X-Linked
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16.320 Level: 2
C16.320.322.500
X-Linked Intellectual Disability
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16.320.322 Level: 3 Tree Number: C16.320.322.500
C16
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C (Diseases) Level: 0
C16.320
Genetic Diseases, Inborn
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16 Level: 1
C16.320.400
Heredodegenerative Disorders, Nervous System
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16.320 Level: 2 Tree Number: C16.320.400
C16
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C (Diseases) Level: 0
C16.320
Genetic Diseases, Inborn
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16 Level: 1
C16.320.565
Metabolism, Inborn Errors
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16.320 Level: 2 Tree Number: C16.320.565
C16
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C (Diseases) Level: 0
C16.320
Genetic Diseases, Inborn
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16 Level: 1
C16.320.565
Metabolism, Inborn Errors
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16.320 Level: 2 Tree Number: C16.320.565
C16
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C (Diseases) Level: 0
C16.320
Genetic Diseases, Inborn
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16 Level: 1
C16.320.565
Metabolism, Inborn Errors
Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities Parent: C16.320 Level: 2 Tree Number: C16.320.565
C18
Nutritional and Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C (Diseases) Level: 0
C18.452
Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C18 Level: 1
C18.452.132
Brain Diseases, Metabolic
Category: Nutritional and Metabolic Diseases Parent: C18.452 Level: 2 Tree Number: C18.452.132
C18
Nutritional and Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C (Diseases) Level: 0
C18.452
Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C18 Level: 1
C18.452.132
Brain Diseases, Metabolic
Category: Nutritional and Metabolic Diseases Parent: C18.452 Level: 2 Tree Number: C18.452.132
C18
Nutritional and Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C (Diseases) Level: 0
C18.452
Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C18 Level: 1
C18.452.648
Metabolism, Inborn Errors
Category: Nutritional and Metabolic Diseases Parent: C18.452 Level: 2 Tree Number: C18.452.648
C18
Nutritional and Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C (Diseases) Level: 0
C18.452
Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C18 Level: 1
C18.452.648
Metabolism, Inborn Errors
Category: Nutritional and Metabolic Diseases Parent: C18.452 Level: 2 Tree Number: C18.452.648
C18
Nutritional and Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C (Diseases) Level: 0
C18.452
Metabolic Diseases
Category: Nutritional and Metabolic Diseases Parent: C18 Level: 1
C18.452.648
Metabolism, Inborn Errors
Category: Nutritional and Metabolic Diseases Parent: C18.452 Level: 2 Tree Number: C18.452.648
C19
Endocrine System Diseases
Category: Endocrine System Diseases Parent: C (Diseases) Level: 0
C19.053
Adrenal Gland Diseases
Category: Endocrine System Diseases Parent: C19 Level: 1
C19.053.500
Adrenal Insufficiency
Category: Endocrine System Diseases Parent: C19.053 Level: 2 Tree Number: C19.053.500
ADE Molecular Mechanism Mapping

Drug-ADE-Human Protein Triplets

Molecular mechanism triplets showing drug-adverse event-protein relationships

4 Total Triplets
4 High Confidence
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Personalized Drug-Protein-ADE Network

Comprehensive Information for Personalized ADE

Comprehensive Information and Reliability for Drug-ADE Association

Drug Confidence Filter
DTA Confidence Level
Layout Style
Show Labels
Total Drugs
11
0 High | 3 Medium | 8 Low Confidence
Total Proteins
6
Target proteins associated with this ADE
Drug-Protein-ADE association
829
0 Known | 4 High | 0 Middle | 825 Low Confidence
Confidence Profile
0%
Known/High/Middle-confidence interactions

This interactive network visualization shows the relationships between the top 50 drugs (ranked by case number) out of 11 total drugs associated with this adverse event, their known and potential off-target proteins, and the associated adverse effect. The connections indicate binding interactions and mechanistic pathways.

Adverse Drug Event (ADE)
Drug
Protein
Drug-Center
Human Protein-Center
confidence level

Drug Confidence Level Distribution

Drug Type Distribution

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Pharmacological Target Class Distribution

Top 8 Function Target Sub Classes

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The Introduction of Drug-AE Confidence Score Grade
Priority Level Score Range Description Evidence Characteristics
High Score ≥ 6.67
High-priority associations requiring immediate attention.
Strong evidence across multiple dimensions with high statistical significance, robust association measures, and substantial case numbers. Warrant priority pharmacovigilance action. High P-value scores (significant Adjust-P), Strong ROR/PRR values, Substantial case numbers, Complete dimensional coverage, Minimal data filtering needed.
Medium 3.33 ≤ Score < 6.67
Medium-priority associations requiring careful evaluation.
Moderate evidence quality with acceptable statistical significance and association strength. May need additional validation or monitoring before definitive action. Moderate P-value significance, Reasonable ROR/PRR measures, Adequate case numbers, Partial dimensional coverage, Some data quality considerations.
Low Score < 3.33
Low-priority associations with limited evidence strength.
May represent weak signals, insufficient data, or associations requiring extensive additional investigation before any regulatory or clinical consideration. Weak P-value significance, Low association measures, Limited case numbers, Incomplete dimensional data, Significant data filtering applied.
PersDTA overview
The Introduction of Drug-AE Severity Score Grade
Severity Level Score Range Description Typical outcomes
Minimal 0 ≤ Score ≤ 0.387
Low severity ADRs requiring minimal intervention.
Events that need medical attention to prevent permanent damage but without hospitalization or life-threatening consequences. Primarily RI (Required Intervention) outcomes, Outpatient management, Preventive measures, Early intervention prevents escalation.
Mild 0.387 < Score ≤ 0.861
Mild severity events requiring hospitalization.
Mix of intervention-required and hospitalization cases with manageable clinical outcomes and good recovery potential. Mix of RI and HO outcomes, Initial or prolonged hospitalization, Active medical management, Generally favorable prognosis.
Moderate 0.861 < Score ≤ 1.500
Moderate ADRs resulting in permanent disability.
Higher proportion of hospitalization and disability cases requiring intensive medical management and long-term care planning. Increased HO and DS outcomes, Permanent disability, Extended hospitalization, Rehabilitation required, Long-term functional impairment.
Severe 1.500 < Score ≤ 2.52
High severity life-threatening events with significant morbidity.
Notable presence of disability and life-threatening outcomes requiring emergency intervention and intensive care management. Prominent DS and LT outcomes, Life-threatening events, Emergency intervention required, ICU admission, High risk of permanent consequences.
Critical 2.524 < Score ≤ 5.000
Critical life-threatening or fatal ADRs with maximum clinical impact.
High proportion of life-threatening events and deaths with very strong drug-event associations requiring immediate regulatory action. Significant LT and DE outcomes, Fatal events, Emergency life-support measures, Immediate drug discontinuation, Regulatory safety alerts.
The Introduction of Drug-AE-Protein Confidence Score Grade
Confidence Level Relationships Description Evidence Types
Known/Valid Direct DTA relationships The drug-ADE, drug-target, and target-ADE associations are all derived from the same literature source. Experimental validation, Clinical evidence
High DT + TA + DA Two of the three associations (drug-ADE, drug-target, and target-ADE) are derived from the same literature source, while the third is validated by other literature. Multiple corroborating sources
Medium DT + TA + DA Two of the three associations (drug-ADE, drug-target, and target-ADE) are validated by separate literature sources. Partial evidence chain
Low TA + DT Only target-ADE and drug-target associations are validated by literature sources. Associative evidence only
Personalized ADE

Route and Formulation-specified Associations

Pharmaceutic Granularity for Route and Formulation specification

Administration Routes (Total: 6 cases across 2 routes)

Dosage Forms (Total: 6 cases across 2 forms)

Drug Route Analysis
Drug Form Analysis

Drug Route Analysis

Route Drug Name Case Number Confidence Score Confidence Level Severity Score Severity Level Details
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Drug Form Analysis

Form Drug Name Case Number Confidence Score Confidence Level Severity Score Severity Level Details
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Disease-stratified Associations

Personalized Granularity for Disease and Indication Stratification

Indication Name
Drug Name
Case Number
Confidence Score
Confidence Level
Severity Score
Severity Level
Details