Rare Disease Library

CAD-CDG

CDG-Iz · Congenital disorder of glycosylation type 1z

CADDS

Contiguous ABCD1 DXS1357E deletion syndrome · Zellweger-like contiguous gene deletion syndrome

CADINS disease

CARD11-associated atopy with dominant interference of NF-kB signaling syndrome

Cold agglutinin disease

CAD · CAS

Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy

CADASIL · Hereditary multi-infarct dementia

Chronic acquired demyelinating polyneuropathy

CADP

Immunodeficiency due to a complement cascade component deficiency

Immunodeficiency due to a complement cascade protein anomaly