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Disease

Autosomal dominant primary hypomagnesemia with hypocalciuria

Also known as HOMG2, Isolated autosomal dominant hypomagnesemia, Isolated renal magnesium wasting, Renal hypomagnesemia type 2.

9
Associated genes
1
Related proteins

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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

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Associated genes

9 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

CLDN160.63CNNM20.53FXYD20.52AGPAT10.06SLC41A30.06SERINC30.05ACSM2A0.04ACSM2B0.04GAR10.04

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Sodium/potassium-transporting ATPase subunit gammavia FXYD20.52

Reference

Authoritative identity, definition & identifiers.

Synonyms

HOMG2, Isolated autosomal dominant hypomagnesemia, Isolated renal magnesium wasting, Renal hypomagnesemia type 2

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.