Griscelli syndrome
ORPHA:381Absent thumb-short stature-immunodeficiency syndrome
ORPHA:2951Acquired immunodeficiency
ORPHA:310050Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency
ORPHA:444463Autoinflammatory syndrome with immune deficiency
ORPHA:290839Combined immunodeficiency due to DOCK8 deficiency
ORPHA:217390Combined immunodeficiency due to partial RAG1 deficiency
ORPHA:231154Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Familial hyperinflammatory lymphoproliferative immunodeficiency
ORPHA:619953Hepatic veno-occlusive disease-immunodeficiency syndrome
ORPHA:79124ICF syndrome
ORPHA:2268Immunodeficiency syndrome with autoimmunity
ORPHA:169355Laron syndrome with immunodeficiency
ORPHA:220465Nijmegen breakage syndrome
ORPHA:647OBSOLETE: Other complex syndrome of primary immunodeficiency
ORPHA:183716Periodic fever-immunodeficiency-thrombocytopenia syndrome
ORPHA:652522Primary immunodeficiency
ORPHA:101997Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency
ORPHA:90023Rh deficiency syndrome
ORPHA:71275Severe intellectual disability and progressive spastic paraplegia
ORPHA:280763Short-limb skeletal dysplasia with severe combined immunodeficiency
ORPHA:935Syndrome with combined immunodeficiency
ORPHA:331217Vici syndrome
ORPHA:1493Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome
ORPHA:568056Wiskott-Aldrich syndrome
ORPHA:906X-linked central congenital hypothyroidism with late-onset testicular enlargement
ORPHA:329235X-linked lymphoproliferative disease due to XIAP deficiency
ORPHA:538934