Channelopathy-associated congenital insensitivity to pain, autosomal recessive
Also known as channelopathy-associated CIP, insensitivity to pain, congenital, neuropathy, hereditary sensory and autonomic, type IID, CIP+7 more
channelopathy-associated CIP, insensitivity to pain, congenital, neuropathy, hereditary sensory and autonomic, type IID, CIP, HSAN2D, HSAN2D, AR, asymbolia for pain, congenital analgesia, autosomal recessive, indifference to pain, congenital, autosomal recessive, insensitivity to pain, channelopathy-associated, neuropathy, hereditary sensory and autonomic, type 2D.
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.
channelopathy-associated CIP, insensitivity to pain, congenital, neuropathy, hereditary sensory and autonomic, type IID, CIP, HSAN2D, HSAN2D, AR, asymbolia for pain, congenital analgesia, autosomal recessive, indifference to pain, congenital, autosomal recessive, insensitivity to pain, channelopathy-associated, neuropathy, hereditary sensory and autonomic, type 2D
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.