Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000220904 Individual ID 00287166 Associated disease BARTS3 Phenotype details salt wasting, hypokalaemia, metabolic alkalosis, Growth delay, polyhydramnios, asthenia Diagnosis/Initial Bartter syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite Bartter syndrome type 3 Age/Examination 00y06m (6 months) Age/Diagnosis - Age/Onset 00y06m Phenotype/Onset 6m Protein - Owner name Dr Silvana Tedeschi Database submission license No license selected Created by Dr Silvana Tedeschi Date created 2020-02-13 14:04:05 +01:00 (CET) Date last edited 2020-02-17 16:42:59 +01:00 (CET)

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