glucosephosphate dehydrogenase deficiency
Information
- Disease name
- glucosephosphate dehydrogenase deficiency
- Disease ID
- DOID:2862
- Description
- "A carbohydrate metabolic disorder that is characterized by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH)." [url:http\://en.wikipedia.org/wiki/Glucosephosphate_dehydrogenase_deficiency]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT00004381 | Completed | Phase 2 | Phase II Randomized Study of Tin Mesoporphyrin for Neonatal Hyperbilirubinemia | December 1999 | |
NCT00076323 | Completed | N/A | A Test to Predict the Hemolytic Potential of Drugs in G6PD Deficiency | December 2003 | November 2006 |
- Disase is a (Disease Ontology)
- DOID:2978
- Cross Reference ID (Disease Ontology)
- GARD:6520
- Cross Reference ID (Disease Ontology)
- MESH:D005955
- Cross Reference ID (Disease Ontology)
- NCI:C98933
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:124134002
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C2939465
- Exact Synonym (Disease Ontology)
- deficiency of G-6PD
- Exact Synonym (Disease Ontology)
- Glucose-6-phosphate dehydrogenase deficiency
- MeSH unique ID (MeSH (Medical Subject Headings))
- D005955