ZFIN Human Disease: familial episodic pain syndrome 1

OBO ID: DOID:0111729

Term Name:	familial episodic pain syndrome 1		Search Ontology:
Synonyms:	FEPS1
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. https://www.ncbi.nlm.nih.gov/pubmed/20547126
References:	OMIM:615040 ORDO:391389
Ontology:	Human Disease ( DOID:0111729 )

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 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TRPA1	trpa1a trpa1b	?Episodic pain syndrome, familial, 1	615040

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None