FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term adrenoleukodystrophy ID (Ontology) DOID:10588 (Human Disease)
Definition A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death.
Also Known As "ALD" ; "Bronze Schilder disease" ; "diffuse sclerosis" (for all, see Synonyms field below)
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Annotations
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       5
Human Disease Models (FBhh)  DOID       2
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 adrenoleukodystrophy       5      4      2
 for disease ribbon | adrenoleukodystrophy       --       1       --
 model of | adrenoleukodystrophy       5      1       --
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
cerebral degeneration           |
 |__leukodystrophy______________|
                                adrenoleukodystrophy  11 rec.
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Is a X-linked recessive disease
leukodystrophy
Part of
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Synonyms
  • "ALD" EXACT OMO:0003012
    "Bronze Schilder disease" EXACT
    "diffuse sclerosis" EXACT
    "Encephalitis periaxialis concentrica" EXACT
    "Encephalitis periaxialis, Schilder's" EXACT
    "Siemerling-Creutzfeldt Disease" EXACT
    "sudanophilic cerebral sclerosis" EXACT
    "X-linked adrenoleukodystrophy" EXACT
Secondary IDs
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ICD10CM:E71.52
MESH:D000326
MIM:300100
NCI:C61252
SNOMEDCT_US_2023_03_01:65389002
UMLS_CUI:C0162309