| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Tuberculosis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Polyneuropathy with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Failure to thrive in infant with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Pneumonia with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Blindness with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Infective arthritis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Candidiasis of mouth with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Thrombocytopenia with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Encephalopathy with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Respiratory disorder with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Strongyloidiasis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Myocarditis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Noninfectious gastroenteritis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Central nervous disorder with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Neuritis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Encephalomyelitis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Herpes zoster with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Neuralgia with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Dyspnea with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Low vision with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Hyperhidrosis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Malignant neoplasm with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Coccidioidomycosis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Cholangitis with acquired immunodeficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 3 | 
| Infectious disease with acquired immune deficiency syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Benign granulocytopenia in childhood | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Febrile granulocytopenia | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Complement component 8 deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Basophilic leukemia | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Hemophagocytic lymphohistiocytosis due to infection | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Agranulocytosis caused by antithyroid agent | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| X-linked lymphoproliferative disease due to SH2D1A deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| X-linked lymphoproliferative disease due to XIAP deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| X-linked severe congenital neutropenia | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Differentiation syndrome due to and following chemotherapy co-occurrent with acute promyelocytic leukemia | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| X-linked agammaglobulinemia with growth hormone deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Mendelian susceptibility to mycobacterial disease | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Bronchiolitis obliterans syndrome due to and following allogeneic stem cell transplant | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 5 | 
| Bronchiolitis obliterans syndrome due to and after lung transplantation | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 5 | 
| Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Severe combined immunodeficiency due to linker for activation of T cells deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Combined immunodeficiency due to moesin deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Combined immunodeficiency due to GINS complex subunit 1 deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Combined immunodeficiency due to transferrin receptor deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| B-cell expansion with nuclear factor kappa light chain enhancer of activated B cells and T-cell anergy disease | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Familial hemophagocytic lymphohistiocytosis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Macrophage activation syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Macrophage activation syndrome due to juvenile systemic onset arthritis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Pediatric multiple sclerosis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Pediatric multiple sclerosis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Leukocyte adhesion deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Leukocyte adhesion deficiency - type 1 | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Leukocyte adhesion deficiency - type 2 | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Phosphoglucomutase 3-related congenital disorder of glycosylation | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Reticular dysgenesis with congenital aleukocytosis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Reticular dysgenesis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Severe combined immunodeficiency with reticular dysgenesis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 6 | 
| Wiskott-Aldrich autosomal dominant variant syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 5 | 
| Combined immunodeficiency due to dedicator of cytokinesis 8 deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Susceptibility to infection due to tyrosine kinase 2 deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Primary immunodeficiency with multifaceted aberrant lymphoid immunity | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Dedicator of cytokinesis 2 deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Susceptibility to localized juvenile periodontitis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Functional disorder of polymorphonuclear neutrophil | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Periodic fever, infantile enterocolitis, autoinflammatory syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Chronic nonbacterial osteomyelitis/chronic recurrent multifocal osteomyelitis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Chronic nonbacterial osteomyelitis/chronic recurrent multifocal osteomyelitis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Primary cutaneous plasmacytosis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to protein tyrosine phosphatase receptor type C deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Severe combined immunodeficiency due to coronin 1A deficiency | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Cytokine release syndrome due to chimeric antigen receptor T-cell immunotherapy | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 5 | 
| Immune effector cell-associated neurotoxicity syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 2 | 
| Autoinflammatory disease | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Familial Mediterranean fever | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Familial amyloid nephropathy with urticaria AND deafness | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 7 | 
| Chronic infantile neurological, cutaneous and articular syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Hereditary periodic fever | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Tumor necrosis factor receptor-associated periodic fever syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Hyper-immunoglobulin D periodic fever syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Cryopyrin associated periodic syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Autoinflammation, lipodystrophy and dermatosis syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Nucleotide binding oligomerization domain containing 2-associated autoinflammatory disease | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Monogenic autoinflammatory syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| NLR family pyrin domain containing 12-associated hereditary periodic fever syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Periodic fever, infantile enterocolitis, autoinflammatory syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 7 | 
| Sterile multifocal osteomyelitis with periostitis and pustulosis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Autoinflammation phospholipase C gamma 2 associated antibody deficiency and immune dysregulation | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 1 | 
| Pyoderma gangrenosum, acne, suppurative hidradenitis syndrome | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 5 | 
| Infantile onset panniculitis with uveitis and systemic granulomatosis | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 | 
| Deficiency of interleukin 36 receptor antagonist | Pathological process | True | Abnormal immune process | Inferred relationship | Existential restriction modifier | 4 |