Term Name: glycogen storage disease XI
Synonyms: lactate dehydrogenase A deficiency
Definition: A glycogen storage disease that has_material_basis_in homozygous mutation in the LDHA gene, which encodes lactate dehydrogenase, on chromosome 11p15.
Ontology: Human Disease [DOID:0061286]   ( DOID:0061286 )

Relationships
is a type of: autosomal recessive disease glycogen storage disease