Phenotypes for disease #02315 (SCIDB (immunodeficiency, severe combined, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative), OMIM:600802)

1 entry on 1 page. Showing entry 1.
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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     
0000122530 - - - Unknown - - - - - Sinem Firtina 00150106
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