Disease #03370 (HP3 (hyperoxaluria, primary, type III (HP3)), OMIM:613616)
Official abbreviation |
HP3 |
Name |
hyperoxaluria, primary, type III (HP3) |
OMIM ID |
613616 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
16 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
HOGA1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-10-22 08:30:18 +02:00 (CEST) |
Individuals
|