Phenotypes for disease #00349 (CFID (deficiency, complement factor I), OMIM:610984)

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     
0000350537 Recurrent infections CFI deficiency CFID Familial, autosomal recessive - - - - - Nima Parvaneh 00464538
0000350538 Recurrent infections C3 deficiency CFID Familial, autosomal recessive - - - - - Nima Parvaneh 00464539
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