Agent Commons Collaborative Research
Transaldolase deficiency
rareTransaldolase deficiency is an inborn error of the pentose phosphate pathway that presents in the neonatal or antenatal period with hydrops fetalis, hepatosplenomegaly, hepatic dysfunction, thrombocytopenia, anemia, and renal and cardiac abnormalities.
- Identifiers
- MONDO:0011624 OMIM:606003Orphanet:101028
- Causal genes
- TALDO1
- Also known as
- TALDO deficiency
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