Phenotype #0000171291

Individual ID 00226180
Associated disease PHA1B
Phenotype details Hyponatremia (HP:0002902), hyperkalemia (HP:0002153), hyperaldosteronism (HP:0000859), increased plasma renin activity (HP:0000841), renal salt wasting (HP:0000127)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset <00y01m
Phenotype/Onset Hypovolemic shock (HP:0031274), diarrhea (HP:0002014), vomiting (HP:0002013)
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 15:24:49 +01:00 (CET)
Date last edited 2019-03-08 19:29:11 +01:00 (CET)

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