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Human Disease

megalencephalic leukoencephalopathy with subcortical cysts 2A

Term ID
DOID:0080318
Synonyms
Definition
A megalencephalic leukoencephalopathy with subcortical cysts characterized by infantile-onset macrocephaly and later onset of motor deterioration, with ataxia and spasticity, seizures, cognitive decline of variable severity, white matter abnormalities, including swelling of the cerebral white matter and subcortical cysts that has_material_basis_in homozygous or compound heterozygous mutation in the HEPACAM gene on chromosome 11q24. (2)
References
Ontology
Human Disease   ( DOID:0080318 )
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