Hypomagnesemia 3, Renal (HOMG3)

Alias:

Homg3

Fhhnc Without Severe Ocular Involvement

Renal Hypomagnesemia Type 3

Primary Hypomagnesemia

Renal Hypomagnesemia 3

Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Without Severe Ocular Involvement

Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Without Severe Ocular Involvement

Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Without Severe O

Hypomagnesemia, Primary, Due to Defect in Renal Tubular Transport of Magnesium

Primary Hypomagnesemia Due to Defect in Renal Tubular Transport of Magnesium

Hypomagnesemia, Familial, with Hypercalciuria and Nephrocalcinosis

Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Renal Hypomagnesemia Hypercalciuria Nephrocalcinosis

Hypomagnesemia, Isolated Renal

Isolated Renal Hypomagnesemia

Hypomagnesemia, Type 3, Renal

Hypomagnesemia 3

Fhhnc

Hhn

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hypomagnesemia 3, Renal, also known as homg3, is related to hypomagnesemia 2, renal and hypomagnesemia 1, intestinal, and has symptoms including abdominal pain, polyuria and seizures. An important gene associated with Hypomagnesemia 3, Renal is CLDN16 (Claudin 16), and among its related pathways/superpathways is Diuretics Pathway, Pharmacodynamics. The drugs Temsirolimus and Benzocaine have been mentioned in the context of this disorder. Affiliated tissues include kidney and liver, and related phenotypes are polydipsia and hypercalciuria

Related ID：

MALACARDS：HYP534

OMIM：248250

MESH：D009397