All individuals with variants in gene MYH2

35 entries on 1 page. Showing entries 1 - 35.
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00002674 - PubMed: Darin 1998, PubMed: Martinsson 2000 large family, 19 affecteds - no Sweden - - - - - CMYO6;MYPOP autosomal dominant inclusion body myopathy, joint contractures, ophthalmoplegia, rimmed vacuoles 1 19 Homa Tajsharghi
00002917 - PubMed: Tajsharghi 2010 - M no United Kingdom (Great Britain) - - - - - Healthy/Control - 1 1 Homa Tajsharghi
00002919 - PubMed: Tajsharghi 2010 - F no United Kingdom (Great Britain) - >41y - - - CMYO6;MYPOP pronounced opthalmoplegia; ptosis; ... 2 1 Homa Tajsharghi
00002920 - PubMed: Tajsharghi 2010 - F no United Kingdom (Great Britain) - >42y - - - CMYO6;MYPOP pronounced opthalmoplegia; no ptosis; ... 2 1 Homa Tajsharghi
00002921 - PubMed: Tajsharghi 2010 - M no United Kingdom (Great Britain) - >44y - - - CMYO6;MYPOP pronounced opthalmoplegia; no ptosis; ... 2 1 Homa Tajsharghi
00002925 - PubMed: Tajsharghi 2010 - M no Finland - >58y - - - CMYO6;MYPOP pronounced opthalmoplegia; no ptosis; ... 2 1 Homa Tajsharghi
00002928 - PubMed: Tajsharghi 2010 - M no Finland - >59y - - - CMYO6;MYPOP pronounced opthalmoplegia; ptosis; ... 2 1 Homa Tajsharghi
00002930 - PubMed: Lossos 2013 affected-1 from families - yes Israel Arab - - - - CMYO6;MYPOP - 2 1 Homa Tajsharghi
00002931 - PubMed: Lossos 2013 affected-2 from families - yes Israel Arab - - - - CMYO6;MYPOP - 2 1 Homa Tajsharghi
00002932 - PubMed: Lossos 2013 unaffected carrier mother F ? Israel - - - - - Healthy/Control - 1 1 Homa Tajsharghi
00002933 - PubMed: Lossos 2013 affected individual M ? Israel - - - - - CMYO6;MYPOP - 2 1 Homa Tajsharghi
00183065 23033978-Trio66 PubMed: de Ligt 2012 - M - Netherlands - - - - - ID see paper; … 1 1 Johan den Dunnen
00208556 - - - F - Germany - - - - - - HP:0003546 (Exercise intolerance); HP:0001263 (Global developmental delay); HP:0000602 (Ophthalmoplegia) 1 1 Andreas Laner
00210171 - - - M - Germany - - - - - - HP:0011804 (Abnormality of muscle physiology); HP:0003326 (Myalgia) 1 1 Andreas Laner
00265572 Dys86-1 PubMed: Izumi 2015 - - - Japan - - - - - MD see paper; … 1 1 Johan den Dunnen
00291616 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 17 Mohammed Faruq
00291617 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00291618 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291619 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 226 Mohammed Faruq
00304555 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 15 Mohammed Faruq
00305877 165438 - - M ? Germany - - - - - IBM 16 year old patient with hyperChemia 933 U/l, scoliosis (mild), indirect hyperbilirubinemia (2.2 mg/dl); HPO: Scoliosis , Elevated serum creatine kinase , Unconjugated hyperbilirubinemia 2 1 Andreas Laner
00307313 - - - M - - - - - - - ? Tetraplegia/tetraparesis (HP:0030182) 1 1 Andreas Laner
00327040 - - - M - France - - - - - MYOP Distal muscle weakness HP:0002460; Elevated serum creatine kinase HP:0003236 1 1 Svetlana Gorokhova
00374408 S-4875 PubMed: Ganapathy 2019 - - - India - - - - - ? Alternating esotropia, myopathy and congenital myathenia 1 1 Johan den Dunnen
00374508 S-4250 PubMed: Ganapathy 2019 - - - India - - - - - ? Muscular dystrophy 1 1 Johan den Dunnen
00374785 S-3956 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00385552 Fam2Pat4 PubMed: Ritelli 2018 - F - Italy - - - - - CHTD facial dysmorphism; hearing loss/recurrent otitis; heart anomalies; mitral valve dystrophy/insufficiency; tricuspid valve dystrophy/insufficiency.; aortic valve dystrophy/insufficiency; atrial septum aneurysm; arrhythmias; other soft connective tissues; abnormal skin texture; joint hypermobility; habitus/orthopedics; short stature; short limbs; neurinoma; palmoplantar keratoderma 1 1 Johan den Dunnen
00388611 Pat47 PubMed: Chakravorty 2020 - M - India India - - - - MYOP distal muscle weakness, proximal muscle weakness; difficulty running, change in gait, wasting of calves, biceps lump; most-affected muscles: Gastrocnemius, Iliopsoas, hip adductors, hamstrings, and quadriceps; cardiac involvement; 35y-ambulant 1 1 Johan den Dunnen
00388670 Pat71 PubMed: Chakravorty 2020 - M - India India - - - - MYOP proximal muscle weakness; CK level 791 IU/L; Tripping and toe walking, Winging of scapula, wrist and ankle contractures; Most-affected muscles: Biceps brachii, ankle dorsiflexors; no cardiac involvement; 11y-ambulant 1 1 Johan den Dunnen
00392024 MDCRC/2119/DBI-1683 PubMed: Karthikeyan 2024 - M yes India - - - yes - DMD delayed fine motor development (HP:0010862), calf muscle hypertrophy (HP:0008981), Gowers sign (HP:0003391), frequent falls (HP:0002359), difficulty climbing stairs (HP:0003551), difficulty walking (HP:0002355), waddling gait (HP:0002515), proximal muscle weakness (HP:0003701), toe walking (HP:0040083) 1 1 Lakshmi Bremadesam
00435182 257846 - - M no Germany - - - - - CMYO6;MYPOP Axial muscle weakness, Skeletal muscle atrophy, Motor delay, Poor suck, Difficulty descending stairs, Strabismus 2 1 Andreas Laner
00436354 SMC1A-Pat2 PubMed: Yuan 2019 2-generation family, 1 affected, unaffected non-carrier parents F - - - - - - - CDLS, MYOP - 1 1 Johan den Dunnen
00442710 Pat82 PubMed: Westra 2019 - M - - - - - - - NMD - 1 1 Johan den Dunnen
00442726 Pat98 PubMed: Westra 2019 - F - - - - - - - NMD Hypotonia, exercise intolerance, muscle weakness, congenital contractures 1 1 Johan den Dunnen
00442757 Pat129 PubMed: Westra 2019 - M - - - - - - - NMD Distal muscle weakness, polyneuropathy, and atrophy of lower legs 1 1 Johan den Dunnen
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