Search Ontology:
Human Disease
glycogen storage disease XI
- Term ID
- DOID:0061286
- 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. https://pubmed.ncbi.nlm.nih.gov/7449146/
- References
- Ontology
- Human Disease ( DOID:0061286 )
Other Pages
Genes Involved
Zebrafish Models