Phenotype #0000222654
Individual ID |
00289019 |
Associated disease |
neuropathy, optic |
Phenotype details |
Hypertension (HP:0000822); Renal insufficiency (HP:0000083) |
Diagnosis/Initial |
- |
Diagnosis/Definite |
- |
Inheritance |
Familial, autosomal dominant |
Age/Examination |
62y (62 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Khadidja Guehlouz |
Database submission license |
No license selected |
Created by |
Khadidja Guehlouz |
Date created |
2020-02-25 12:13:14 +01:00 (CET) |
Date last edited |
2020-08-25 21:27:59 +02:00 (CEST) |
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