Disease #00012 (HP3 (Hyperoxaluria, Primary, Type III), OMIM:613616)
Official abbreviation |
HP3 |
Name |
Hyperoxaluria, Primary, Type III |
OMIM ID |
613616 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
HOGA1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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