Multiple Mitochondrial Dysfunctions Syndrome 2
Disease ID: disease_node_16814
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| Dbxref | GARD:12632, MIM:614299, ORDO:401874 |
|---|---|
| Subclassof | DOID_0050737, DOID_0070330 |
| Data Source | DOID |
| Synonyms | BOLA3 deficiency, multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia |
| Doid Label | multiple mitochondrial dysfunctions syndrome 2 |
| Doid Description | 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. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16814 |
| Doid Id | DOID_0080134 |
| Label | Multiple Mitochondrial Dysfunctions Syndrome 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)