Disease

multiple mitochondrial dysfunctions syndrome 2

Definition
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
  • BOLA3 deficiency
  • multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

Associated Alleles

No data available

Associated Models

No data available