| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Chédiak-Higashi syndrome | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Chronic granulomatous disease | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hereditary lymphedema | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Acquired epidermolysis bullosa | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Wiskott-Aldrich syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hypopigmentation-immunodeficiency disease | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Familial C3B inhibitor deficiency syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hand-Schüller-Christian disease | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Adenosine deaminase deficiency | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Purine-nucleoside phosphorylase deficiency | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| X-linked agammaglobulinemia | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| X-linked lymphoproliferative syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Storage disease of the lung | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hereditary angioedema | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Autosomal recessive severe combined immunodeficiency disease | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Complement component deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Severe combined immunodeficiency disease | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Acatalasemia | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Chronic granulomatous disease | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Familial sea-blue histiocytosis | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Triglyceride storage disease with ichthyosis | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hereditary white blood cell disorder | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| X-linked agammaglobulinemia with growth hormone deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Ataxia-telangiectasia syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hereditary angioedema with normal C1 esterase inhibitor activity | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Microcephaly, normal intelligence and immunodeficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Common variable immunodeficiency with autoantibodies to B- or T-cells | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Vici syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Absent thumb with short stature and immunodeficiency syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Schimke immuno-osseous dysplasia | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Pyogenic arthritis, pyoderma gangrenosum, acne syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Anhidrotic ectodermal dysplasia with immune deficiency | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Lichtenstein syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Isolated agammaglobulinemia | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Constitutional mismatch repair deficiency syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Combined immunodeficiency due to OX40 deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Combined immunodeficiency with faciooculoskeletal anomalies syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Vasculitis due to adenosine deaminase 2 deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Facial dysmorphism, immunodeficiency, livedo, short stature syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Roifman syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Neonatal inflammatory skin and bowel disease | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Deficiency in anterior pituitary function, variable immunodeficiency syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Sterile multifocal osteomyelitis with periostitis and pustulosis | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Osteopetrosis hypogammaglobulinemia syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Severe dermatitis, multiple allergies, metabolic wasting syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Primary CD59 deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| STING-associated vasculopathy with onset in infancy | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability with seizure and psoriasis syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Recurrent Neisseria infection due to factor D deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Immunodeficiency with factor I anomaly | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Deficiency of interleukin 36 receptor antagonist | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Genetically determined myasthenia | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hennekam lymphangiectasia-lymphedema syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency | Is a | False | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Familial granulomatous inflammatory arthritis, dermatitis and uveitis | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Complement component 3 deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Autoimmune lymphoproliferative syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hereditary C1 esterase inhibitor deficiency - deficient factor | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Hereditary C1 esterase inhibitor deficiency - dysfunctional factor | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Familial cold urticaria | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Polyglandular autoimmune syndrome, type 1 | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| X-linked immunoneurologic disorder | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Infantile inflammatory bowel disease with neurological involvement | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Familial chilblain lupus erythematosus | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Autoimmune interstitial lung disease, arthritis syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Familial amyloid nephropathy with urticaria AND deafness | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Autoinflammation, lipodystrophy and dermatosis syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| NLR family pyrin domain containing 12-associated hereditary periodic fever syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Autoinflammation phospholipase C gamma 2 associated antibody deficiency and immune dysregulation | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  | 
| Ubiquitin specific peptidase 18 deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Existential restriction modifier |  |