Renal hypomagnesemia 2
Also known as FXYD2 familial primary hypomagnesemia, FXYD2 primary hypomagnesemia, HOMG2, familial primary hypomagnesemia caused by mutation in FXYD2+8 more
FXYD2 familial primary hypomagnesemia, FXYD2 primary hypomagnesemia, HOMG2, familial primary hypomagnesemia caused by mutation in FXYD2, isolated autosomal dominant hypomagnesemia, isolated renal magnesium wasting, primary hypomagnesemia caused by mutation in FXYD2, renal hypomagnesemia type 2, autosomal dominant primary hypomagnesemia with hypocalciuria, hypomagnesemia 2, renal, magnesium loss, isolated renal, magnesium wasting, renal.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
FXYD2 familial primary hypomagnesemia, FXYD2 primary hypomagnesemia, HOMG2, familial primary hypomagnesemia caused by mutation in FXYD2, isolated autosomal dominant hypomagnesemia, isolated renal magnesium wasting, primary hypomagnesemia caused by mutation in FXYD2, renal hypomagnesemia type 2, autosomal dominant primary hypomagnesemia with hypocalciuria, hypomagnesemia 2, renal, magnesium loss, isolated renal, magnesium wasting, renal
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.