All individuals with variants in gene RYR3

12 entries on 1 page. Showing entries 1 - 12.
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00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00291177 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 66 Mohammed Faruq
00291179 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291180 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291181 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 33 Mohammed Faruq
00304459 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00304460 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00427800 Pat188 PubMed: Zhou 2018 family, 1 affected, unaffected carrier father M - China - - - - - epilepsy intellectual disability; generalized tonic-clonic seizure, tonic, complex partial seizure, frequency 1-3/wk; EEG burst of fast activity, generalized spike wave; resistant to antiepileptic drugs 1 1 Johan den Dunnen
00472655 Pat59 PubMed: Estevez-Arias 2025 patient - - - - - - - - NMD - 1 1 Johan den Dunnen
00472930 Fam203735Pat27 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history M no Iran - - - - - MYOP Two affected patients, proximal lower muscle weakness, gait disturbance, myogenic pattern in EMG, flat feet, negative IHC for all examined antibodies and focal fiber type grouping reported in muscle biopsy. 2 1 Johan den Dunnen
00473245 Fam112232Pat449 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - MYOP onset 3y, Difficulty climbing steps; Muscle spasm; Respiratory muscle weakness; Gowers sign; EMG-NCV: suggestive of myotonic myopathy, R/O chronic myositis; Elevated CPK, LDH & Aldolase levels; Muscle biopsy: myopathic atrophy with some necrotic and degenerative/regenerative fibers and some small foci of perivascular chronic inflammation; IHC: gamma sarcoglycan with weak sarcolemmal labelling of all muscle fibers; Echocardiography: classic MVP, trivial MR & TR. There is parental consanguinity with absence of family history. 1 1 Johan den Dunnen
00473354 Fam206226Pat620 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MYOP bilateral ptosis, mild facial weakness, generalized muscle weakness, gait abnormality, exercise intolerance, fatigue, sarcolemmal labelling of all examined antibodies 1 1 Johan den Dunnen
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