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 1 ID (Ontology) DOID:0111729 (Human Disease)
Definition A familial episodic pain syndrome characterized by onset in infancy of episodic debilitating upper body pain triggered by fasting, cold, and physical stress that has_material_basis_in heterozygous mutation in the TRPA1 gene on chromosome 8q13.
Also Known As "FEPS1"
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 Genes
 familial episodic pain syndrome 1       3
 for disease ribbon | familial episodic pain syndrome 1       3
 model of | familial episodic pain syndrome 1       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_______
neuropathy                           |
 |__familial episodic pain syndrome__|
                                     familial episodic pain syndrome 1  3 rec.
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Is a autosomal dominant disease
familial episodic pain syndrome
Part of
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Synonyms
  • "FEPS1" EXACT OMO:0003012
Secondary IDs
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MIM:615040
ORDO:391389