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Disease

Hereditary sensory and autonomic neuropathy type 7

Late-stage therapeutic development
Also known as CIP with hyperhidrosis and gastrointestinal dysfunction, HSAN VII, HSAN with hyperhidrosis and gastrointestinal dysfunction, HSAN7+9 more

CIP with hyperhidrosis and gastrointestinal dysfunction, HSAN VII, HSAN with hyperhidrosis and gastrointestinal dysfunction, HSAN7, SCN11A autosomal dominant hereditary sensory and autonomic neuropathy, autosomal dominant hereditary sensory and autonomic neuropathy caused by mutation in SCN11A, congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction, hereditary sensory and autonomic neuropathy type VII, hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction, HSAN 7, insensitivity to pain, congenital, with gastrointestinal dysfunction and hyperhidrosis, neuropathy, hereditary sensory and autonomic, type 7, neuropathy, hereditary sensory and autonomic, type VII.

24
Clinical trials
1
Associated genes
1
Related proteins

What's happening now

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

Major developments
Clinical Milestones10View all 10
+2 more in the activity timeline below
Activity timeline10

Clinical trials

18 sponsors · 5 new · 3 completed in the last 12 months (net +4)

The current development programme across all trial phases.

Clinical programme
24
All trials
6
Active
18
Late-stage
6
Completed
Late-stage studies
Recruiting
Recently completed

Associated genes

1 match

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

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.

Reference

Authoritative identity, definition & identifiers.

Synonyms

CIP with hyperhidrosis and gastrointestinal dysfunction, HSAN VII, HSAN with hyperhidrosis and gastrointestinal dysfunction, HSAN7, SCN11A autosomal dominant hereditary sensory and autonomic neuropathy, autosomal dominant hereditary sensory and autonomic neuropathy caused by mutation in SCN11A, congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction, hereditary sensory and autonomic neuropathy type VII, hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction, HSAN 7, insensitivity to pain, congenital, with gastrointestinal dysfunction and hyperhidrosis, neuropathy, hereditary sensory and autonomic, type 7, neuropathy, hereditary sensory and autonomic, type VII

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.