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DO Term : familial episodic pain syndrome 2 [DOID:0111730] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A familial episodic pain syndrome characterized by adult-onset of paroxysmal pain mainly affecting the distal lower extremities that has_material_basis_in heterozygous mutation in the SCN10A gene on chromosome 3p22.
  • synonyms:
  • OMIM:615551,
  • 615551,
  • FEPS2
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents