DO_rare_slim has material basis in autosomal recessive disease leukoencephalopathy with vanishing white matter DOID:0060868 MIM:PS603896 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. ORDO:157713 ORDO:157719 ORDO:157716 ORDO:99853 CACH/VWM ORDO:135 ORDO:157719 ORDO:157713 ORDO:157716 ICD10CM:E75.2 childhood ataxia with central nervous system hypomyelination disease_ontology CACH GARD:231 ovarioleukodystrophy vanishing white matter leukodystrophy leukodystrophy autosomal recessive inheritance