Phenotypes for disease #02214

1 entry on 1 page. Showing entry 1.
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AscendingPhenotype ID     

Phenotype details     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

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Owner     

Individual ID     
0000138573 - X-linked congenital spinal muscular atrophy SMAX-2 Familial, X-linked recessive - - - ? - Alfons Meindl 00173709
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