Phenotypes for disease #02250 (CNMX (myopathy, centronuclear, X-linked (CNMX)), OMIM:310400)

7 entries on 1 page. Showing entries 1 - 7.
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Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

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Individual ID     
0000060519 Myotubular myopathy, X-linked (OMIM:310400) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080950
0000160451 Severe myotubular myopathy CNMX Familial - - <1m Severe neonatal weakness, global hypotonia and abolished tendon reflexes - Jorge Oliveira 00211970
0000231796 - - - Familial, X-linked recessive - - - - - Sha Hong 00305947
0000351471 Decreased fetal movement (HP:0001558), Premature (HP:0001622) (birth at 31 weeks), Neonatal hypotonia (HP:0001319) (with predominant bulbar muscle weakness), Respiratory failure requiring assisted ventilation (HP:0004887), Ophthalmoparesis (HP:0000597) - CNMX Familial, X-linked recessive - 00y04m 00y00m congenital onset - María Eugenia Foncuberta 00466085
0000351745 - Myopathy with joint contractures Myopathy, centronuclear, X-linked Familial, autosomal dominant - - - - - Camille Verebi 00466382
0000361822 HP:0001290 (Generalized hypotonia); HP:0001324 (Muscle weakness); HP:0001558 (Decreased fetal movement) myopathy CNMX Familial, X-linked recessive - - - - - Lucia Rodriguez-Noriega Béjar 00477215
0000362727 Progressive proximal muscle weakness, facial involvement, hypotonia since childhood, delayed motor milestones, loss of independent ambulation in adulthood, scapular winging, kyphoscoliosis, dysphagia. Muscle MRI shows diffuse fatty infiltration. Muscle biopsy demonstrates fibro-fatty replacement without classical centronuclear features. Undiagnosed myopathy CNMX Familial, X-linked <01y 49y - - - Arystan Zhakupbekov 00478126
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