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Disease

Hereditary sensory and autonomic neuropathy type 4

Late-stage therapeutic development
Also known as CIP-anhidrosis syndrome, HSAN4, Hereditary Sensory and Autonomic Neuropathy Type IV, NTRK1 hereditary sensory and autonomic neuropathy+14 more

CIP-anhidrosis syndrome, HSAN4, Hereditary Sensory and Autonomic Neuropathy Type IV, NTRK1 hereditary sensory and autonomic neuropathy, congenital insensitivity to pain with anhidrosis, congenital insensitivity to pain-anhidrosis syndrome, hereditary sensory and autonomic neuropathy caused by mutation in NTRK1, hereditary sensory and autonomic neuropathy type IV, hereditary sensory neuropathy type IV, insensitivity to pain, congenital, with anhidrosis, CIPA, HSAN 4, HSAN IV, HSNAN4, familial dysautonomia, type 2, hereditary sensory and autonomic neuropathy 4, hereditary sensory neuropathy type 4, neuropathy, congenital sensory, with anhidrosis.

24
Clinical trials
2
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 Milestones11View all 11
+3 more in the activity timeline below
Activity timeline11

Clinical trials

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

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

2 matches

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-anhidrosis syndrome, HSAN4, Hereditary Sensory and Autonomic Neuropathy Type IV, NTRK1 hereditary sensory and autonomic neuropathy, congenital insensitivity to pain with anhidrosis, congenital insensitivity to pain-anhidrosis syndrome, hereditary sensory and autonomic neuropathy caused by mutation in NTRK1, hereditary sensory and autonomic neuropathy type IV, hereditary sensory neuropathy type IV, insensitivity to pain, congenital, with anhidrosis, CIPA, HSAN 4, HSAN IV, HSNAN4, familial dysautonomia, type 2, hereditary sensory and autonomic neuropathy 4, hereditary sensory neuropathy type 4, neuropathy, congenital sensory, with anhidrosis

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.