01
AGXT
alanine--glyoxylate and serine--pyruvate aminotransferase
alanine--glyoxylate and serine--pyruvate aminotransferase
Diseases
Hyperoxaluria, Primary, Type I
hyperoxaluria, primary, type i
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Hyperoxaluria, Primary, Type I
- Standard Disease Name
- hyperoxaluria, primary, type i
- MeSH Tree
- No data
- ICD-10
- E74.8
Identifiers
- DO ID
- No data
- MeSH ID
- C536414
- OMIM ID
- 259900
- UMLS ID
- C0268164
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NICHD_1602D:Recessively inherited primary hyperoxaluria due to alanine-glyoxylate aminotransferase (AGXT) deficiency.|NCI2016_02D:Recessively inherited primary hyperoxaluria due to alanine-glyoxylate aminotransferase (AGXT) deficiency.(NICHD)