Phenotypes for disease #04158 (alpha-actinin-3 deficiency, OMIM:102574)

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     
0000021619 2/5 individuals with congenital muscular dystrophy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00025500
0000021621 ACTN3 staining muscle negative - - Familial, autosomal recessive - - - - - Johan den Dunnen 00025501
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