Phenotypes for disease #02806

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     
0000120779 nude severe T-cell immunodeficiency with normal B and NK cells, thymus dysgenesis, congenital alopecia and nail dystrophy - - Familial, autosomal recessive 00y06m 00y06m - nude SCID - Sinem Firtina 00148287
0000122513 Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive - - Familial, autosomal recessive 00y09m - - - - Sinem Firtina 00150111
0000122531 - - - Unknown - - - - - Sinem Firtina 00150107
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