Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Benign combined immunodeficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Severe combined immunodeficiency disease |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Vici syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Absent thumb with short stature and immunodeficiency syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to calcium release activated calcium channel dysfunction |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Immuno-osseous dysplasia |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Laron syndrome with immunodeficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to OX40 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Susceptibility to respiratory infection associated with CD8alpha chain mutation |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency with faciooculoskeletal anomalies syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive lymphoproliferative disease |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to serine/threonine kinase 4 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Facial dysmorphism, immunodeficiency, livedo, short stature syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Severe dermatitis, multiple allergies, metabolic wasting syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
T-cell receptor alpha-beta-positive T-cell deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Pancytopenia due to IKAROS family zinc finger 1 mutations |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency with granulomatosis |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to interleukin 21 receptor deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Hennekam lymphangiectasia-lymphedema syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to moesin deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to GINS complex subunit 1 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to transferrin receptor deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
B-cell expansion with nuclear factor kappa light chain enhancer of activated B cells and T-cell anergy disease |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to CD70 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Phosphoglucomutase 3-related congenital disorder of glycosylation |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to dedicator of cytokinesis 8 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency, enteropathy spectrum |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency due to lipopolysaccharide-responsive beige-like anchor protein deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Primary immunodeficiency with multifaceted aberrant lymphoid immunity |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Dedicator of cytokinesis 2 deficiency |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome |
Is a |
True |
Combined immunodeficiency disease |
Inferred relationship |
Existential restriction modifier |
|