Disease #01487 (PEPD (pain disorder, paroxysmal, extreme (PEPD)), OMIM:167400)

Official abbreviation PEPD
Name pain disorder, paroxysmal, extreme (PEPD)
OMIM ID 167400
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SCN9A
Associated tissues -
Disease features autosomal dominant
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00152082 - PubMed: Jarecki 2008 - - - - - - 0 - - PEPD - SCN9A SCN9A 1 1 Christoph Lossin
00152083 - PubMed: Jarecki 2008 - - - - - - 0 - - PEPD - SCN9A SCN9A 1 1 Christoph Lossin
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