OBO ID: DOID:0070372
Term Name: leukoencephalopathy with vanishing white matter 3 Search Ontology:
Synonyms:
Definition: A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B3 gene on chromosome 1p34. (2)
References:
Ontology: Human Disease   ( DOID:0070372 )
Relationships
is a type of:
OTHER leukoencephalopathy with vanishing white matter 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EIF2B3 Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure 620313
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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