Indifference to Pain, Congenital, Autosomal Recessive (CIP)

Alias:
Neuropathy, Hereditary Sensory and Autonomic, Type Iid
Asymbolia for Pain
Cip
Insensitivity to Pain, Channelopathy-Associated
Channelopathy-Associated Insensitivity to Pain
Congenital Indifference to Pain
Channelopathy-Associated Congenital Insensitivity to Pain, Autosomal Recessive
Channelopathy-Associated Congenital Insensitivity to Pain
Pain, Indifference, Congenital, Autosomal Recessive
Congenital Analgesia, Autosomal Recessive
Congenital Analgesia Autosomal Recessive
Insensitivity to Pain, Congenital
Pain Insensitivity, Congenital
Congenital Pain Indifference
Congenital Analgesia
Cip-Scn9a
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Indifference to Pain, Congenital, Autosomal Recessive, also known as neuropathy, hereditary sensory and autonomic, type iid, is related to generalized epilepsy with febrile seizures plus, type 7 and neuropathy, hereditary sensory and autonomic, type iia. An important gene associated with Indifference to Pain, Congenital, Autosomal Recessive is SCN9A (Sodium Voltage-Gated Channel Alpha Subunit 9). The drugs Levobupivacaine and Ropivacaine have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and tongue, and related phenotypes are pain insensitivity and intellectual disability
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Unknown
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1
16
27

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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