All diseases

OMIM ID
133020
OMIM term:
ERYTHERMALGIA, PRIMARY
Alternative terms:
ERYTHROMELALGIA, PRIMARY
ERYTHROMELALGIA, FAMILIAL NEUROPATHY, SMALL FIBER, INCLUDED; SFNP, INCLUDED
(∗) Location:
2q24.3  
(†) Associated OMIM genes:
SCN9A  
(‡) Associated MGI genes:

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