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Disease Ontology Browser
leukoencephalopathy with vanishing white matter (DOID:0060868)
Alliance: disease page
Synonyms: CACH; CACH/VWM; childhood ataxia with central nervous system hypomyelination; ovarioleukodystrophy; vanishing white matter leukodystrophy
Alt IDs: ICD10CM:E75.2, OMIM:PS603896, ORDO:135, ORDO:157713, ORDO:157716, ORDO:157719
Definition: A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory