Phenotypes for disease #01108 (MDDGB2 (dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B2), OMIM:613156)

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     
0000334284 HP:0003560 Muscular dystrophy HP:0001263 Global developmental delay HP:0001319 Neonatal hypotonia HP:0003701 Proximal muscle weakness HP:0003236 Elevated circulating creatine kinase concentration HP:0030099 Reduced muscle fiber alpha dystroglycan - MDDGB2 Familial, autosomal recessive - - - - - María Eugenia Foncuberta 00445032
0000334329 HP:0003560 Muscular dystrophy HP:0001263 Global developmental delay HP:0001319 Neonatal hypotonia HP:0003701 Proximal muscle weakness HP:0003236 Elevated circulating creatine kinase concentration HP:0011968 Feeding difficulties - - Familial, autosomal recessive - - - neonatal - María Eugenia Foncuberta 00445076
0000346536 HP:0001385 Hip dysplasia (3 m), HP:0001319 Neonatal hypotonia, HP:0003560 Global developmental delay, HP:0003701 Proximal muscle weakness, HP:0003236 Elevated circulating creatine kinase concentration, HP:0000252 microcephaly; HP:0030099 Reduced muscle fiber alpha dystroglycan in her sister muscle biospy - MDDGB2 Familial, autosomal recessive 01y07m - - - - María Eugenia Foncuberta 00458089
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