Search Ontology:
Human Disease

primary hyperoxaluria type 3

Term ID
DOID:0111672
Synonyms
  • HP3
  • PH III
  • primary hyperoxaluria type III
Definition
A primary hyperoxaluria characterized by recurring calcium oxalate stones that has_material_basis_in homozygous or compound heterozygous mutation in the HOGA1 gene on chromosome 10q24.2. (2)
References
  • GARD:10738
  • NCI:C123214
  • OMIM:613616
  • ORDO:93600
  • SNOMEDCT_US_2023_03_01:734990008
  • UMLS_CUI:C3150878
Ontology
Human Disease   ( DOID:0111672 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations