Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Autosomal recessiv svær kombineret immundefekt |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
X-bundet svær kombineret immundefekt |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency with maternofetal engraftment |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Warts, hypogammaglobulinaemia, infections, and myelokathexis |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Benign combined immunodeficiency |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
SCID due to absent IL-2 receptor |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder) |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent adenosine deaminase (disorder) |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Adenosine deaminase deficiency (disorder) |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent interleukin-2 production (disorder) |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent T cell receptor (disorder) |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Nezelof's syndrome |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
SCID forårsaget af manglende klasse II HLA-antigener |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency with reticular dysgenesis (disorder) |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency with low T- and B-cell numbers |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency with low or normal B-cell numbers |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
major histokompatibilitetskompleksmangel, klasse I |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
A rare autosomal recessive primary immunodeficiency characterized by absence of HLA class II molecules on the surface of immune cells, leading to severely impaired cellular and humoral immune response to foreign antigens, severe CD4+ T-cell lymphopenia, and hypogammaglobulinemia. The disease clinically manifests with early onset of severe and recurrent infections mainly of the respiratory and gastrointestinal tract, protracted diarrhea with failure to thrive, and autoimmune disease, and is frequently fatal in childhood. |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Kombineret immundefekt, ikke nærmere specificeret |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Autosomal recessive severe combined immunodeficiency disease (disorder) |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency (SCID) due to DNA-PKcs deficiency is an extremely rare type of SCID characterized by the classical signs of SCID (severe and recurrent infections, diarrhea, failure to thrive), absence of T and B lymphocytes, and cell sensitivity to ionizing radiation. |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
This syndrome is characterized by severe immunodeficiency, osteopetrosis, lymphedema and anhidrotic ectodermal dysplasia. |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
Severe combined immunodeficiency (SCID) due to gamma chain deficiency, also called SCID-X1, is a form of SCID characterized by severe and recurrent infections, associated with diarrhea and failure to thrive. |
Is a |
False |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|
A group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T lymphocytes with presence of B lymphocytes, resulting in early-onset severe respiratory viral, bacterial, or fungal infections, diarrhea and failure to thrive. |
Is a |
True |
Severe combined immunodeficiency disease |
Inferred relationship |
Some |
|