OBO ID: DOID:0111730 |
Term Name: | familial episodic pain syndrome 2 | Search Ontology: | |
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Synonyms: |
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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: | |||
Ontology: | Human Disease ( DOID:0111730 ) |
OTHER familial episodic pain syndrome 2 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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SCN10A | Episodic pain syndrome, familial, 2 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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