All individuals with variants in gene CPT2

26 entries on 1 page. Showing entries 1 - 26.
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00035446 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00035447 - - - - - Germany - - - - - ? suspected defect of CPT2, rhabdomyolysis, myalgias and weakness 1 1 Andreas Laner
00035448 - - - - - Germany - - - - - ? relapsing myalgias 1 1 Andreas Laner
00064759 SIDS001 PubMed: Neubauer 2017, Journal: Neubauer 2017 - F ? Switzerland Europe 00y09m - - - SIDS SIDS 1 1 Cordula Haas
00095882 - - - - - - - - - - - carnitine palmitoyltransferase II deficiency, late-onset carnitine palmitoyl transferase II deficiency myopathic form (CPT2, adult-onset form); rhabdomyolysis (HP:0003201) 1 1 Daniela Avila-Smirnow
00265254 - - - F - Spain - - - - - carnitine palmitoyltransferase II deficiency, late-onset - 2 1 Jorge Docampo Cordeiro
00274449 Pat157 PubMed: Park 2017 - M - Korea - - - - - MD Ankle dorsiflexor weakness; elevated CK (793 IU/L); no family history 1 1 Johan den Dunnen
00289877 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00289878 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00289879 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 133 Mohammed Faruq
00289880 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00289881 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00301524 - - 2 affected sisters F ? Greece - - - - - CPT II deficiency, infantile - 1 2 Helen Latsoudis
00301525 - - 2 affected siblings (1M, 1F) M no Greece - 17y - - - CPT II deficiency, infantile - 1 2 Helen Latsoudis
00304209 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 17 Mohammed Faruq
00314189 - PubMed: Topf 2020 analysis 1001 patients with unexplained limb-girdle weakness - - - - - - - - LGMD - 1 1 Johan den Dunnen
00314190 - PubMed: Topf 2020 analysis 1001 patients with unexplained limb-girdle weakness - - - - - - - - LGMD - 1 1 Johan den Dunnen
00442770 Pat142 PubMed: Westra 2019 - M - - - - - - - NMD Myopathy and cardiac conduction abormalites 1 1 Johan den Dunnen
00457637 Pat1 PubMed: Diekman 2014 - M - Netherlands - - - - - ? see paper; ..., muscle pain (after exercise); normal muscle power during neurological exam 1 1 Johan den Dunnen
00457638 Pat2 PubMed: Diekman 2014 - M - Netherlands - - - - - ? see paper; ..., exercise intolerance, muscle pain (after exercise); normal muscle power during neurological exam 1 1 Johan den Dunnen
00457639 Pat3 PubMed: Diekman 2014 - M - Netherlands - - - - - ? see paper; ..., exercise intolerance, muscle pain; normal muscle power during neurological exam 2 1 Johan den Dunnen
00472247 - Verebi et al. (submitted) - M - France - - - - - carnitine palmitoyltransferase II deficiency, late-onset 0003326: Myalgia, 0003710: Muscle cramps during exercise 1 1 Camille Verebi
00472499 Pat1 PubMed: Mohamed 2026 - F - United Kingdom (Great Britain) - - - - - ? see paper; ..., recurrent episodes acute rhabdomyolysis, black urine; raised creatine kinase (5,000 IU/L); longstanding history muscle fatigue/aching legs following vigorous activities; physical examination entirely normal. 1 1 Johan den Dunnen
00473065 Fam13637Pat180 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MYOP onset 7y with muscle cramps in lower limbs following exercise; Episodic weakness with myoglobinuria; Mild calf muscles pseudohypertrophy; Elevated CPK; Normal EMG-NCV; Muscle biopsy: no significant histochemical pathologic finding, no lipid or glycogen excess. 1 1 Johan den Dunnen
00473755 Fam9609806Pat1207 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M no Iran - - - - - MYOP Rhabdomyolysis; Muscle pain & weakness following vigorous activities; Amblyopia, Lt. eye; and Elevated level of serum CK. EMG-NCV findings are compatible with myopathic process, Mc Ardle disease (glycogenosis, type V) 1 1 Johan den Dunnen
00473863 Fam9803414Pat1362 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M no Iran - - - - - MYOP onset 8y, Muscle cramps following exercise or fasting; Muscle weakness following exercise. 1 1 Johan den Dunnen
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