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

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

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
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