All individuals with variants in gene PNPLA2

11 entries on 1 page. Showing entries 1 - 11.
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00036537 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00208766 - - - M - Germany - - - - - - HP:0003198 (Myopathy) 2 1 Andreas Laner
00290554 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00324477 patient PubMed: Avila-Smirnow 2020 2-generation family, 1 affected unaffected heterozygous carrier parents F yes Chile - - - - - ? see paper; ..., congenital hypotonia, mother polyhydramnios during pregnancy, delayed acquisition of motor milestones, hepatomegaly, elevated creatine kinase levels, lipid accumulation muscle fibers, Jordans’ anomaly blood smear 1 1 Johan den Dunnen
00460266 Pat37 PubMed: Marti 2025 patient, family history - - Spain - - - - - hCK asymptomatic, hyperCKemia; elevated CK level 1000-2300 UI/L; lipids drops; MRI muscle normal; EMG normal 1 1 Johan den Dunnen
00472969 Fam9611127Pat66 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - MYOP Myopia; Muscle weakness, upper/lower limbs; Positive history for papillary thyroid Cancer; EMG-NCV: myopathic process with prominently spontaneous activity in all examined muscles; Antibodies to Gangliosids: negative; Elevated level of CPK & Aldolase; Muscle biopsy: lipid storage myopathy 2 1 Johan den Dunnen
00473007 Fam1410Pat105 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MYOP Asymmetric proximal & distal muscle weakness from 6y ago; Diabetes mellitus; Muscle pain; Neck muscle weakness; Difficulty running, walking & raising arms; Limb muscle atrophy; Elevated SGOT, SGPT & CPK; Echocardiography: mild diastolic LV dysfunction; EMG-NCV: chronic myopathy with some irritations; Polycythemia, suspicious of ; Muscle biopsy: vacuolar myopathy with necrosis/regeneration, lipid excess and presence of some rimmed vacuoles. 1 1 Johan den Dunnen
00473156 Fam103322Pat302 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - MYOP onset at age of 32y with Difficulty running & Lower limb muscle weakness; Calf muscle pseudohypertrophy; Fasciculations; Gowers sign; Hypoesthesia; Paresthesia; EMG-NCV: irritable myopathy; Elevated CPK & LDH. Above clinical information is based on HPO nomenclature. 1 1 Johan den Dunnen
00473958 Fam9909938Pat1490 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MYOP Proximal muscle weakness, upper/lower; Cardiomyopathy, LV systolic & diastolic dysfunction & mild TR; Elevated level of CPK; Muscle biopsy suggestive of lipid storage myopathy. 1 1 Johan den Dunnen
00479464 ARMD348 PubMed: Nallamilli 2023 - M - United States - - - - - NMD not specified 1 1 Johan den Dunnen
00479465 ARMD349 PubMed: Nallamilli 2023 - F - United States - - - - - NMD not specified 1 1 Johan den Dunnen
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