ZFIN Human Disease: familial episodic pain syndrome 2

OBO ID: DOID:0111730

Term Name:	familial episodic pain syndrome 2		Search Ontology:
Synonyms:	FEPS2
Definition:	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. https://www.ncbi.nlm.nih.gov/pubmed/23115331
References:	OMIM:615551
Ontology:	Human Disease ( DOID:0111730 )

Relationships

is a type of:	autosomal dominant disease familial episodic pain syndrome autosomal dominant disease familial episodic pain syndrome Show first 5 Terms

OTHER familial episodic pain syndrome 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SCN10A		Episodic pain syndrome, familial, 2

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None