Statements (11)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
neurological symptoms
mitochondrial disease lactic acidosis |
| gptkbp:fullName |
Pyruvate Dehydrogenase Complex Assembly Deficiency
|
| https://www.w3.org/2000/01/rdf-schema#label |
PDHAD
|
| gptkbp:location |
human chromosome X
|
| gptkbp:relatedTo |
gptkb:pyruvate_dehydrogenase_complex
PDHA1 gene |
| gptkbp:bfsParent |
gptkb:PDHA1
|
| gptkbp:bfsLayer |
7
|