Disease #01958 (CNM2 (myopathy, centronuclear, type 2 (CNM-2)), OMIM:255200)

Official abbreviation CNM2
Name myopathy, centronuclear, type 2 (CNM-2)
OMIM ID 255200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 1 gene BIN1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00144462 17676042-AAT68 PubMed: Nicot 2007 2-generation family, 3 affected sibs, unaffected heterozygous carrier parents M yes India - >12y - - - CNM2 reduced fetal movements, oligohydramnios, intra-uterine growth retardation; muscle weakness proximal, slowly progressive, ptosis, contractures at birth, normal intelligence BIN1 BIN1 1 3 Johan den Dunnen
00144463 17676042-ACC82 PubMed: Nicot 2007 sister of AAT68 F yes India - 01y - - - CNM2 reduced fetal movements, oligohydramnios, intra-uterine growth retardation; muscle weakness proximal, contractures at birth; hypodevelopment frontal lobes; died from viral myocarditis BIN1 BIN1 1 1 Johan den Dunnen
00144464 17676042-ADS5 PubMed: Nicot 2007 sister of AAT68 F yes India - 00y00m01d - - - CNM2 - BIN1 BIN1 1 1 Johan den Dunnen
00144465 17676042-ADR71 PubMed: Nicot 2007, PubMed: Toussaint 2010 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Iraq - >35y - - - CNM2 normal pregnancy; muscle weakness proximal BIN1 BIN1 1 1 Johan den Dunnen
00144466 17676042-LF41 PubMed: Nicot 2007 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Iraq - >14y - - - CNM2 normal pregnancy; muscle weakness proximal, slowly progressive, facial weakness, ptosis, ophtalmoparesis BIN1 BIN1 1 1 Johan den Dunnen
00144495 20142620-Pat PubMed: Claeys 2010, PubMed: Toussaint 2010 2-generation family, 1 affected, unaffected heterozygous carrier father M - Morocco - - - - - CNM2 - BIN1 BIN1 1 1 Johan den Dunnen
00144496 20476667-Pat PubMed: Mejaddam 2009 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Sweden - >17y - - - CNM2 wheelchair-bound 13y BIN1 BIN1 1 1 Johan den Dunnen
00144498 ? PubMed: Toussaint 2010 - - - - - - - - - CNM2 centronuclear myopathy; 12y-disease stable BIN1 BIN1 1 1 Johan den Dunnen
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