All individuals with variants in gene LMOD3

28 entries on 1 page. Showing entries 1 - 28.
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00027154 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 1a; 2-generation family, 2 affecteds sisters, unaffected heterozygous carrier parents F yes Algeria - <00y00m28d - - - NEM severe congenital nemaline myopathy; deceased (neonatal period, <28d); polyhydramnios, preterm delivery (30/40), arthrogryposis, fractures (bilateral femoral) 1 2 Johan den Dunnen
00027155 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 1b F yes Algeria - <00y00m28d - - - NEM severe congenital nemaline myopathy; deceased (neonatal period, <28d); preterm delivery (36/40) 1 1 Johan den Dunnen
00027156 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents M ? Belgium - 10m - - - NEM severe congenital nemaline myopathy; decreased fetal movements, breech presentation, arthrogryposis, ophthalmoplegia 1 1 Johan den Dunnen
00027157 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 3a; 2-generation family, 2 affecteds sisters, unaffected heterozygous carrier parents F ? Portugal - <00y00m28d - - - NEM severe congenital nemaline myopathy; deceased (neonatal period); polyhydramnios, decreased fetal movements, contractures 1 2 Johan den Dunnen
00027158 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents M ? Japan - >4m - - - NEM severe congenital nemaline myopathy; alive 4m, lost to follow-up 1 1 Johan den Dunnen
00027159 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Japan - >2m - - - NEM severe congenital nemaline myopathy; alive 2m, lost to follow-up; polyhydramnios, decreased fetal movements, subdural hematoma 2 1 Johan den Dunnen
00027160 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents F ? Japan - >10m - - - NEM severe congenital nemaline myopathy; alive 10m, lost to follow-up; polyhydramnios, decreased fetal movements, fetal edema, preterm delivery (32/40), microcephaly, contractures 1 1 Johan den Dunnen
00027161 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Japan - >01y07m - - - NEM severe congenital nemaline myopathy; alive 1y7m, lost to follow-up; polyhydramnios, decreased fetal movements, ophthalmoplegia 2 1 Johan den Dunnen
00027162 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents F no - America, south <00y00m28d - - - NEM severe congenital nemaline myopathy; deceased (neonatal period) 2 1 Johan den Dunnen
00027163 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents F ? Italy - 4m - - - NEM severe congenital nemaline myopathy; deceased (4m); polyhydramnios, decreased fetal movements, preterm delivery (34/40), ophthalmoplegia, contractures 1 1 Johan den Dunnen
00027164 - PubMed: Yuen 2014, Journal: Yuen 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Ecuador - 1m15d - - - NEM severe congenital nemaline myopathy; deceased (6w); polyhydramnios, decreased fetal movements, preterm delivery (35/40), breech presentation, ophthalmoplegia, arthrogryposis, fractures (bilateral humeral) 2 1 Johan den Dunnen
00027165 - PubMed: Yuen 2014, Journal: Yuen 2014 brother 11a; 2-generation family, 2 affecteds sisters, unaffected heterozygous carrier parents M ? Sweden - 5m - - - NEM severe congenital nemaline myopathy; deceased (5m); polyhydramnios, arthrogryposis 1 2 Johan den Dunnen
00027166 - PubMed: Yuen 2014, Journal: Yuen 2014 brother 12a; 2-generation family, 2 affecteds sisters, unaffected heterozygous carrier parents M ? Afghanistan - 2m - - - NEM severe congenital nemaline myopathy; deceased (2m); absent fetal movements, preterm delivery (31/40), breech presentation, arthrogryposis 1 3 Johan den Dunnen
00027167 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 13a; 2-generation family, 2 affecteds sisters, unaffected heterozygous carrier parents F ? Pakistan - 3m - - - NEM severe congenital nemaline myopathy; deceased (3m); polyhydramnios, breech presentation, ophthalmoplegia, kyphosis 1 2 Johan den Dunnen
00027168 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 14a; 2-generation family, 2 affecteds sisters, unaffected heterozygous carrier parents F no Australia - >10y - - - NEM typical congenital nemaline myopathy; alive (10y); polyhydramnios, decreased fetal movements, bulbar weakness, ophthalmoplegia, percutaneous endoscopic gastrostomy, nocturnal noninvasive ventilation.; walks independently; normal cardiac assessment and echocardiogram 2 2 Johan den Dunnen
00027169 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 3b F ? Portugal - >1m - - - NEM severe congenital nemaline myopathy; alive 1m, lost to follow-up; polyhydramnios, contractures 1 1 Johan den Dunnen
00027170 - PubMed: Yuen 2014, Journal: Yuen 2014 brother 11b M ? Sweden - <00y00m28d - - - NEM severe congenital nemaline myopathy; deceased (neonatal period) 1 1 Johan den Dunnen
00027171 - PubMed: Yuen 2014, Journal: Yuen 2014 brother 12b M ? Afghanistan - <00y00m28d - - - NEM severe congenital nemaline myopathy; deceased (neonatal period); preterm delivery (33/40), arthrogryposis 1 1 Johan den Dunnen
00027172 - PubMed: Yuen 2014, Journal: Yuen 2014 affected fetus 12c - ? Afghanistan - <0d - - - NEM severe congenital nemaline myopathy; affected fetus 1 1 Johan den Dunnen
00027173 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 13b F ? Pakistan - <00y00m28d - - - NEM severe congenital nemaline myopathy; deceased (neonatal period);polyhydramnios, decreased fetal movements. 1 1 Johan den Dunnen
00027174 - PubMed: Yuen 2014, Journal: Yuen 2014 sister 14b F no Australia - >4y - - - NEM typical congenital nemaline myopathy; alive (4y); polyhydramnios, bulbar weakness, percutaneous endoscopic gastrostomy, nocturnal noninvasive ventilation; walks with truncal support; nNormal cardiac assessment and echocardiogram 2 1 Johan den Dunnen
00293465 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 9 Mohammed Faruq
00293466 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 81 Mohammed Faruq
00293467 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293468 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 56 Mohammed Faruq
00424787 - Segarra-Casas 2022, submitted - F yes Spain - - - - - NEM10 HP:0001270, HP:0002359, HP:0030319, HP:0003690, HP:0003798 1 1 Alba Segarra Casas
00472939 Fam211606Pat36 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M no Iran - - - - - MYOP Sporadic case, started childhood with proximal and distal upper and lower muscle weakness, facial muscle weakness, myopia, foot drop, gait abnormality, bulbar dysfunction and chronic non irritable myopathy reported in EDX 2 1 Johan den Dunnen
00472957 Fam9417255Pat54 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MD Hypotonia at birth; High-arched palate; Muscle weakness, proximal; Joint contractures; Calf pseudohypertrophy; Wheelchair-bound. EMG is compatible with a myopathic process 1 1 Johan den Dunnen
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