FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial episodic pain syndrome 3 ID (Ontology) DOID:0111731 (Human Disease)
Definition A familial episodic pain syndrome characterized by early childhood onset of intense episodic pain mainly affecting the distal lower extremities, but sometimes also the upper extremities, with pain cycles lasting several days and exacerbated by fatigue that has_material_basis_in heterozygous mutation in the SCN11A gene on chromosome 3p22.
Also Known As "FEPS3"
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 Genes
 familial episodic pain syndrome 3       2
 for disease ribbon | familial episodic pain syndrome 3       2
 model of | familial episodic pain syndrome 3       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_______
neuropathy                           |
 |__familial episodic pain syndrome__|
                                     familial episodic pain syndrome 3  2 rec.
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Is a autosomal dominant disease
familial episodic pain syndrome
Part of
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Synonyms
  • "FEPS3" EXACT OMO:0003012
Secondary IDs
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MIM:615552
NCI:C125390
ORDO:391392