Phenotypes for disease #03629 (EMARDD (myopathy, areflexia, respiratory distress, and dysphagia, early-onset), OMIM:614399)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000227601 pectus excavatum, ptosis, fatigue, muscle hypotrophy - congenital myopathy Unknown 61y 61y 50y 15y - Alessandra Govoni 00300292
0000357007 Generalized amyotrophy * Long face * Hypomimic face * Ptosis Abnormality of the voice * Scoliosis * Spinal rigidity * Equinus calcaneus * Velopharyngeal insufficiency * Gastroesophageal reflux * Motor delay * Abnormality of the musculature of the neck * Neonatal hypotonia Congenital myopathy Congenital myopathy Isolated (sporadic) - - - - - Camille Verebi 00472198
0000357019 Distal muscle weakness * Myopathy * Musculotendinous retraction Myopathy with joint contractures Congenital myopathy Isolated (sporadic) - - - - - Camille Verebi 00472210
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