has material basis in autosomal recessive disease immunodeficiency 93 MIM:619705 DOID:0061063 disease_ontology A primary immunodeficiency disease that is characterized by onset of recurrent viral and bacterial infections, particularly with encapsulated bacteria, and hypertrophic cardiomyopathy in the first months or years of life and that has_material_basis_in homozygous or compound heterozygous mutation in the FNIP1 gene on chromosome 5q31. immunodeficiency-93 and hypertrophic cardiomyopathy primary immunodeficiency disease autosomal recessive inheritance