Phenotypes for disease #01553 (EDMD2;LGMD1B (dystrophy, muscular, Emery-Dreifuss, type 2 (EDMD2;LGMD1B)), OMIM:181350)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000046763 cardiac conduction defect - - Unknown - - - - - Yulia Rogozhina 00059233
0000143385 - - - Unknown - - - - - Florence van Tienen 00181217
0000257380 Muscle weakness HP:0001324 - - Unknown - - - - - Ibrahim Sahin 00361988
0000351472 Waddling gait (HP:0002515), Difficulty running (HP:0009046), Difficulty climbing stairs (HP:0003551), Elevated circulating creatine kinase concentration (HP:0003236) (CPK: 346/322 UI/L), Elbow contracture (HP:0034391), Achilles tendon contracture (HP:0001771), Spinal rigidity (HP:0003306) - EDMD2 Familial, autosomal dominant 11y 11y11m - Juvenile onset - María Eugenia Foncuberta 00466086
0000351473 Elbow contracture (HP:0034391), Arrhythmia (HP:0011675) - EDMD2 Familial, autosomal dominant - 35y07m - - - María Eugenia Foncuberta 00466087
0000351778 Achilles tendon contracture Spinal rigidity Contractures of the joints of the upper limbs Contractures of the joints of the lower limbs Contractures of the large joints Follicular hyperkeratosis Myopathy with joint contractures EDMD2 Unknown - - - - - Camille Verebi 00466414
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