Disease #01872 (CIP (pain, indifference, congenital, autosomal recessive (CIP)), OMIM:243000)

Official abbreviation CIP
Name pain, indifference, congenital, autosomal recessive (CIP)
OMIM ID 243000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 16
Phenotype entries for this disease 15
Associated with 1 gene SCN9A
Associated tissues -
Disease features autosomal recessive
Remarks -


Individuals

16 entries on 1 page. Showing entries 1 - 16.
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00080860 - Trujillano et al., submitted unaffected parents - - - - - 0 - - CIP HSAN2D, autosomal recessive (OMIM:243000) SCN9A SCN9A 1 1 Daniel Trujillano
00152075 - PubMed: Cox 2006 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152076 - PubMed: Cox 2006 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152077 - PubMed: Cox 2006 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152078 - PubMed: Cox 2006 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152079 - PubMed: Cox 2006 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152080 - PubMed: Goldberg 2007 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152081 - PubMed: Goldberg 2007 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152087 - PubMed: Nilsen 2009 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152088 - PubMed: Nilsen 2009 - - - - - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152116 - PubMed: Goldberg 2007 - - - Italy - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152117 - PubMed: Goldberg 2007 - - - United States - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152118 - PubMed: Goldberg 2007 - - - Argentina - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00152119 - PubMed: Goldberg 2007 - - - United States - - 0 - - CIP - SCN9A SCN9A 1 1 Christoph Lossin
00155016 1 (YA) PubMed: Danziger 2006 patient 1 (YA) in table 1 F yes France - >44y 0 - - CIP No pain feeling for wounds, burns, bone fractures, appendicitis, deliveries - SCN9A 1 1 Wen He
00218058 19250380-Fam2 PubMed: Suriu 2009 42-generation family, affected sisters, unaffected heterozygous carrier parents/relatives F yes Morocco - - 0 - - CIP see paper; ... NTRK1 NTRK1 1 2 Johan den Dunnen
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