Bartter Syndrome, Type 2, Antenatal (BARTS2)

Alias:

Bartter Disease Type 2

Bartter Syndrome, Type 2

Barts2

Hyperprostaglandin E Syndrome 2

Bartter Syndrome Type 2

Hypokalemic Alkalosis with Hypercalciuria 2, Antenatal

Hypokalemic Alkalosis with Hypercalciuria 2 Antenatal

Hypokalemic Alkalosis with Hypercalciuria Antenatal 2

Antley-Bixler Syndrome, Autosomal Dominant

Bartter Syndrome, Antenatal , Type 2

Bartter Syndrome Type 2 Antenatal

Bartter Syndrome Antenatal Type 2

Hyperprostanglandin E Syndrome 2

Bartter Syndrome 2, Antenatal

Antenatal Bartter Syndrome 2

Bartter Syndrome Type Ii

Bartter Syndrome 2

Abs2

Bs2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Bartter Syndrome, Type 2, Antenatal, also known as bartter disease type 2, is related to nephrocalcinosis and nephrolithiasis, and has symptoms including constipation, diarrhea and fever. An important gene associated with Bartter Syndrome, Type 2, Antenatal is KCNJ1 (Potassium Inwardly Rectifying Channel Subfamily J Member 1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Dopamine-DARPP32 Feedback onto cAMP Pathway. Affiliated tissues include kidney and heart, and related phenotypes are hypomagnesemia and hypokalemia

Related ID：

MALACARDS：BRT050

OMIM：241200

MESH：D001477