Phenotype #0000303453
Individual ID |
00411413 |
Associated disease |
HP1 |
Phenotype details |
stone disease with nephrocalcinosis |
Diagnosis/Initial |
oxalosis |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
Primary hyperoxaluria |
Age/Examination |
08y (8 years) |
Age/Diagnosis |
08y |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Aiysha Abid |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Aiysha Abid |
Date created |
2022-06-13 11:44:46 +02:00 (CEST) |
Date last edited |
2022-06-17 10:57:08 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|