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bn:03564313n
Noun Concept
Categories: Magnesium, Channelopathies, Calcium, Nephrology, Autosomal recessive disorders
EN
hypomagnesemia with secondary hypocalcemia  intestinal hypomagnesemia 1  HOMG1  hypomagnesemia caused by selective magnesium malabsorption  hypomagnesemia intestinal type 1
EN
Hypomagnesemia with secondary hypocalcemia is an autosomal recessive genetic disorder that affects the absorption of magnesium in the intestines. Wikipedia
Definitions
Relations
Sources
EN
Hypomagnesemia with secondary hypocalcemia is an autosomal recessive genetic disorder that affects the absorption of magnesium in the intestines. Wikipedia
Human disease Wikidata
IS A
rare disease
neonatal hypocalcemia
GENETIC ASSOCIATION
TRPM6
Wikipedia
EN
hypomagnesemia with secondary hypocalcemia
Wikidata
EN
intestinal hypomagnesemia 1
Wikidata Alias
EN
HOMG1, hypomagnesemia caused by selective magnesium malabsorption, hypomagnesemia intestinal type 1, hypomagnesemic tetany, intestinal hypomagnesemia with secondary hypocalcemia, primary hypomagnesemia with secondary hypocalcemia

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