Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
May Hegglin syndrome |
Is a |
False |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Severe combined immunodeficiency with reticular dysgenesis |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary eosinophilia |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Chronic granulomatous disease |
Is a |
False |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary hypersegmentation |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Chédiak-Higashi syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Reticular dysgenesis |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Heritable disorder of neutrophil production |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Heritable disorder of neutrophil function |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Fanconi's anemia |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Shwachman syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Periodontitis co-occurrent with infantile genetic agranulocytosis |
Is a |
False |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Cutaneous mastocytosis, short stature, hearing loss syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Revesz syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
WT limb blood syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Ataxia pancytopenia syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Poikiloderma with neutropenia |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Pancytopenia with developmental delay syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Congenital neutropenia, myelofibrosis, nephromegaly syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary isolated aplastic anemia |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary neutrophilia |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Familial hemophagocytic lymphohistiocytosis |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Onycho-tricho-dysplasia neutropenia syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Combined immunodeficiency, enteropathy spectrum |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Periodic fever, infantile enterocolitis, autoinflammatory syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|
Warts, hypogammaglobulinemia, infections, and myelokathexis |
Is a |
True |
Hereditary white blood cell disorder |
Inferred relationship |
Existential restriction modifier |
|