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2 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 2
1 OMIM reference -
3 associated genes
2 signs/symptoms
Sodium channelopathy-related small fiber neuropathy
Paroxysmal extreme pain disorder

SCN10A SCN10A
SCN9A SCN11A
SCN9A


COMMON
GENES
SCN10A
SCN9A



Citations in the biomedical literature:


Sodium channelopathy-related small fiber neuropathy
SCN10A SCN9A
Paroxysmal extreme pain disorder
SCN11A



Sodium channelopathy-related small fiber neuropathy
Paroxysmal extreme pain disorder

Synonym(s):
(no synonyms)

Synonym(s):
- Familial rectal pain

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Paroxysmal extreme pain disorder

Very frequent
- Autosomal dominant inheritance

Frequent
- Constipation



Sodium channelopathy-related small fiber neuropathy

(no data available)