Phenotypes for disease #03888 (SMALED2A (atrophy, muscular, spinal, lower extremity predominant, type 2A), OMIM:615290)

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     
0000245747 HP:0002650 scoliosis; HP:0001760 abnormal foot morphology; HP:0002804 arthrogryposis multiplex congenita; HP:0003202 skeletal muscle atrophy Arthrogryposis multiplex congenita SMALED2B Isolated (sporadic) 21y 21y 00y00m - - Francisco Ribeiro-Mourão 00327457
0000245841 HP:0002747 Respiratory insufficiency due to muscle weakness; HP:0002878 Respiratory failure; HP:0011968 Feeding difficulties;HP:0003202 Skeletal muscle atrophy; HP:0001374 Congenital hip dislocation; HP:0001760 Abnormal foot morphology; HP:0001762 Talipes equinovarus; HP:0002804 Arthrogryposis multiplex congenita;HP:0002119 Ventriculomegaly; HP:0001558 Decreased fetal movement arthrogriposis SMALED2B Familial, autosomal dominant 00y01m 00y01m 00y00m - - Francisco Ribeiro-Mourão 00327589
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