Phenotype #0000171260

Individual ID 00226147
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 Failure to thrive (HP:0001508), vomiting (HP:0002013), dehydration (HP:0001944), feeding difficulties (HP:0008872)
Protein -
Owner name Susan Tzotzos
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Susan Tzotzos
Date created 2019-02-28 13:29:01 +01:00 (CET)
Date last edited 2019-03-08 18:23:11 +01:00 (CET)

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