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Disease Ontology Browser
hypomyelinating leukodystrophy 6 (DOID:0060798)
Alliance: disease page
Synonyms: H-ABC; HABC; HLD6; hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum; hypomyelination with atrophy of basal ganglia and cerebellum
Alt IDs: OMIM:612438, ICD10CM:E75.2, ORDO:139441
Definition: A hypomyelinating leukodystrophy characterized by infant or early childhood onset of delayed motor development and gait instability, followed by extrapyramidal movement disorders, progressive spastic tetraplegia, ataxia, hypomyelination, cerebellar atrophy, and atrophy or disappearance of the putamen that has_material_basis_in heterozygous mutation in the TUBB4A gene on chromosome 19p13.

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
MGI 6.15
The Jackson Laboratory