Phenotypes for disease #04639 (CMS11 (myasthenic syndrome, congenital, type 11, associated with acetylcholine receptor deficiency (CMS-11)), OMIM:616326)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000307756 HP:0000276 Long face HP:0000218 High palate HP:0000508 Ptosis HP:0000338 Hypomimic face HP:0001252 Hypotonia HP:0002098 Respiratory distress (neonatal) HP:0003388 Easy fatigability HP:0002650 Scoliosis (mild) HP:0001558 Decreased fetal movement HP:0001388 Joint laxity Positive response to pyridostigmine - CMS11 (#616326) Familial, autosomal recessive 09y06m 06y06m - Neonatal onset HP:0003623 - María Eugenia Foncuberta 00415980
0000307765 HP:0000431 Wide nasal bridge HP:0001252 Hypotonia HP:0000508 Ptosis HP:0000276 Long face HP:0000218 High palate HP:0001558 Decreased fetal movement HP:0001324 Muscle weakness retraction of Achilles positive response to pyridostigmine - CMS11 (#616326) Familial, autosomal recessive 04y04m 04y04m - - - María Eugenia Foncuberta 00415999
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