Phenotypes for disease #03430 (C1SD (C1s deficiency), OMIM:613783)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000325415 Homozygous probands presenting with Kikuchi-Fujimoto disease (KFD), also named Histiocytic Necrotizing Lymphadenitis, a rare and usually self-limited idiopathic inflammatory disease - - Familial - 16y - - - Christian Drouet 00435215
0000325440 Female proband presenting with recurrent infections (several episodes of pneumonia, septic arthritis and sinusitis) and SLE manifestations since the age of 7 - 25y Familial - - 07y - - Christian Drouet 00435244
0000325447 Proband presenting with a complete C1s deficiency, including LES with malar rash, lupus nephritis, ANA+, dsDNA Ab+, dilated cardiomyopathy at age 26y - 11y Familial - - - - - Christian Drouet 00435251
0000325449 Proband presenting a complete C1s deficiency, with seizures and virus-associated hemophagocytic syndrome at age 4y; death at age 7y - - Familial 04y - - - - Christian Drouet 00435253
0000325450 Homozygous proband and her brother are presenting with a selective C1s deficiency and recurrent infections (several episodes of pneumonia, septic arthritis and sinusitis) and SLE manifestations since age 7y - 25y Familial - - 07y - - Christian Drouet 00435254
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