Channelopathy-associated congenital insensitivity to pain, autosomal recessive

MONDO:0009459

A syndrome characterized by indifference to pain despite the ability to distinguish noxious from non-noxious stimuli. Absent corneal reflexes and intellectual disability may be associated. Familial forms with autosomal recessive and autosomal dominant patterns of inheritance have been described. (Adams et al., Principles of Neurology, 6th ed, p1343)

Also known as: 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

6 clinical trials for this condition and its sub-types, 6 tagged with Channelopathy-associated congenital insensitivity to pain, autosomal recessive itself.

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Where it sits in the disease tree

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↑ Hereditary disease (18235) ↑ Syndromic disease (7158)

Including sub-types (6) Tagged with Channelopathy-associated congenital insensitivity to pain, autosomal recessive (6)

Trials to join now! 3 Not yet recruiting 1 Completed 2

Channelopathy-associated congenital insensitivity to pain, autosomal recessive

Where it sits in the disease tree

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