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
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