Phenotype #0000171287

Individual ID 00226173
Associated disease PHA1B
Phenotype details Hyponatremia (HP:0002902), hyperkalemia (HP:0002153), hyperaldosteronism (HP:0000859), increased plasma renin activity (HP:0000841)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset <00y01m
Phenotype/Onset Dehydration (HP:0001944), jaundice (HP:0000952)
Protein -
Owner name Susan Tzotzos
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Susan Tzotzos
Date created 2019-03-01 13:12:34 +01:00 (CET)
Date last edited 2019-03-08 19:28:07 +01:00 (CET)

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