You are using an outdated browser. Please upgrade your browser to improve your experience.

cryptosporidiosis-chronic cholangitis-liver disease syndrome

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive primary immunodeficiency characterized by B- and T-cell defects and variable dysfunction of NK cells. Patients tend to have normal numbers of lymphocytes, but show defective class-switched B-cells, low IgG, defective antibody response, and defective T-cell responses to certain antigens.
Mondo Term and Equivalent IDs
MONDO:0014082:  cryptosporidiosis-chronic cholangitis-liver disease syndrome
Orphanet:357329: 
UMLS:C3554687: