Phenotype #0000171213

Individual ID 00226106
Associated disease PHA1B
Phenotype details Elevated sweat choride (HP:0012236), dehydration (HP:0001944), hyponatremia (HP:0002902), hyperkalemia (HP:0002153), high plasma renin activity (HP:0000841), hyperaldosteronism (HP:0000859)
Diagnosis/Initial Cystic fibrosis
Inheritance Familial, autosomal recessive
Diagnosis/Definite PHA1B
Age/Examination -
Age/Diagnosis -
Age/Onset 00y06m
Phenotype/Onset Elevated sweat choride (HP:0012236), dehydration (HP:0001944)
Protein -
Owner name Susan Tzotzos
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Susan Tzotzos
Date created 2019-02-26 13:56:01 +01:00 (CET)
Date last edited 2019-02-28 08:33:35 +01:00 (CET)

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