Autosomal dominant pseudohypoaldosteronism type 1
Also known as PHA1A, autosomal dominant PHA 1, pseudohypoaldosteronism type i, autosomal dominant, PHA I, autosomal dominant+5 more
PHA1A, autosomal dominant PHA 1, pseudohypoaldosteronism type i, autosomal dominant, PHA I, autosomal dominant, pseudohypoaldosteronism type 1 autosomal dominant, pseudohypoaldosteronism type 1, dominant, pseudohypoaldosteronism, type I, autosomal dominant, renal PHA1, renal pseudohypoaldosteronism type 1.
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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.
PHA1A, autosomal dominant PHA 1, pseudohypoaldosteronism type i, autosomal dominant, PHA I, autosomal dominant, pseudohypoaldosteronism type 1 autosomal dominant, pseudohypoaldosteronism type 1, dominant, pseudohypoaldosteronism, type I, autosomal dominant, renal PHA1, renal pseudohypoaldosteronism type 1
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.