Human genes for multiple mitochondrial dysfunctions syndrome 2
Multiple mitochondrial dysfunctions syndrome 2 [DOID:0080134]
A multiple mitochondrial dysfunctions syndrome that is characterized by increased serum glycine and lactate, developmental regression in infancy, an encephalopathic disease course with seizures, spasticity, loss of head control, and abnormal movement, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the bolA family member 3 gene on chromosome 2p13.
Synonyms: multiple mitochondrial dysfunctions syndrome 2, DOID:0080134, BOLA3 deficiency, multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia