Visceral neuropathy, familial, 1, autosomal recessive
Also known as Argyrophil myenteric plexus deficiency of, Argyrophil myenteric plexus, deficiency of, NID A, intestinal pseudoobstruction due to neuronal disease+5 more
Argyrophil myenteric plexus deficiency of, Argyrophil myenteric plexus, deficiency of, NID A, intestinal pseudoobstruction due to neuronal disease, neuronal intestinal dysplasia, type a, pseudoobstruction chronic idiopathic intestinal neuronal type, pseudoobstruction, chronic idiopathic intestinal, neuronal type, visceral neuropathy familial, visceral neuropathy, familial, autosomal recessive.
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.
Argyrophil myenteric plexus deficiency of, Argyrophil myenteric plexus, deficiency of, NID A, intestinal pseudoobstruction due to neuronal disease, neuronal intestinal dysplasia, type a, pseudoobstruction chronic idiopathic intestinal neuronal type, pseudoobstruction, chronic idiopathic intestinal, neuronal type, visceral neuropathy familial, visceral neuropathy, familial, autosomal recessive
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.