Term Name: leukodystrophy and cerebellar atrophy
Synonyms: LDCA
Definition: A leukodystrophy characterized by neurodevelopmental defects, leukodystrophy, and cerebellar atrophy that has_material_basis_in homozygous or compound heterozygous mutation in the LSM7 gene on chromosome 19p13.
Ontology: Human Disease [DOID:0070800]   ( DOID:0070800 )

Relationships
is a type of: autosomal recessive disease leukodystrophy