Search Ontology:
Human Disease

hypomyelinating leukoencephalopathy

Term ID
DOID:0050987
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by nystagmus, spasticity, and a distinct pattern of MRI abnormalities. https://www.ncbi.nlm.nih.gov/pubmed/22232354
References
Ontology
Human Disease   ( DOID:0050987 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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