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 |
|