All individuals with variants in gene MYBPC1

9 entries on 1 page. Showing entries 1 - 9.
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00107913 - - - M yes Israel Bedouin - - - - LCCS4 - 1 1 Ginat Narkis
00290569 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00290570 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00442606 FamPatII1 PubMed: Iyer 2024 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Czech Republic - - - - - arthrogryposis HP:0001371, HP:0003121, HP:0100360, HP:0005750, HP:0009473, HP:0001220, HP:0034671, HP:0003273, HP:0000508, HP:0001561 2 1 Barbora Lauerova
00472256 - Verebi et al. (submitted) - F - France - - - - - CMYO16;MYOTREM 0003198: Myopathy, 0009062: Axial hypotonia in infants, 0012389: Appendicular hypotonia, 0002174: Postural tremor, 0002322: Resting tremor, 0007089: Faciolingual fasciculations 1 1 Camille Verebi
00472257 - Verebi et al. (submitted) - M - France - - - - - CMYO16;MYOTREM 0001337: Tremor, 0009020: Exercise-induced muscle fatigue, 0002315: Headache, 0002380: Fasciculations 1 1 Camille Verebi
00473235 Fam111605Pat432 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M no Iran - - - - - CMS Ptosis, since 14-month age; Negative anti-MuSK antibody test; Abnormal jitter analysis. 1 1 Johan den Dunnen
00473812 Fam9704809Pat1284 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - SMA Preterm; Low birth weight; Hypotonia since birth; Respiratory problem since birth; Suspicion of seizure; Nasogastric tube feeding; died 4-mo.; Echocardiography was suggestive of small ASD, and suspicion of VSD, PFO and closing PDA. 1 1 Johan den Dunnen
00473852 Fam9801780Pat1348 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history F yes Iran - - - - - MD Hypotonia since birth; Myopathic face; Generalized muscle weakness; Tremor, generalized; Lordosis; Winged scapula; Abnormality of gait; EMG-NCV: myopathic process; Muscle biopsy: slight type 1 fiber predominance, atrophy with no necrosis and regeneration or specific structural abnormality but prominent peripheral cluster of mitochondria. 1 1 Johan den Dunnen
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