has material basis in germline mutation in BCL10 inborn error of immunity hereditary disease immunodeficiency 37 https://github.com/monarch-initiative/mondo/issues/6186 https://www.malacards.org/card/immunodeficiency_37 Any primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL10 gene. BCL10 is definitively associated with combined immunodeficiency due to BCL10 deficiency. This has been repeatedly demonstrated in both the research and clinical diagnostic settings and has been upheld over time. See linked ticket for more details. This classification was approved by the ClinGen SCID/CID GCEP. GARD:0024994 primary immunodeficiency disease caused by mutation in BCL10 immunodeficiency 37 BCL10 primary immunodeficiency disease UMLS:C4015195 combined immunodeficiency due to BCL10 deficiency MEDGEN:863632 IMD37 immunodeficiency type 37 DOID:0111939 OMIM:616098 MONDO:0014491