DOID:0111969
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immunodeficiency 39
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Aliases:
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Homo sapiens (human)
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DOID:0111968
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immunodeficiency 41
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Aliases:
-
CD25 deficiency
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IL2RA deficiency
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IMD41
-
immunodeficiency 41 with lymphoproliferation and autoimmunity
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immunodeficiency due to CD25 deficiency
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interleukin-2 receptor alpha chain deficiency
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Homo sapiens (human)
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DOID:0111968
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immunodeficiency 41
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Aliases:
-
CD25 deficiency
-
IL2RA deficiency
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IMD41
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immunodeficiency 41 with lymphoproliferation and autoimmunity
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immunodeficiency due to CD25 deficiency
-
interleukin-2 receptor alpha chain deficiency
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Mus musculus (house mouse)
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DOID:0111968
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immunodeficiency 41
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Aliases:
-
CD25 deficiency
-
IL2RA deficiency
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IMD41
-
immunodeficiency 41 with lymphoproliferation and autoimmunity
-
immunodeficiency due to CD25 deficiency
-
interleukin-2 receptor alpha chain deficiency
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Rattus norvegicus (Norway rat)
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DOID:0111967
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immunodeficiency 54
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Aliases:
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IMD54
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NKCD
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familial isolated natural killer cell deficiency
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primary immunodeficiency due to MCM4 deficiency
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primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
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Mus musculus (house mouse)
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DOID:0111967
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immunodeficiency 54
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Aliases:
-
IMD54
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NKCD
-
familial isolated natural killer cell deficiency
-
primary immunodeficiency due to MCM4 deficiency
-
primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
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|
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Homo sapiens (human)
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DOID:0111967
|
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immunodeficiency 54
-
Aliases:
-
IMD54
-
NKCD
-
familial isolated natural killer cell deficiency
-
primary immunodeficiency due to MCM4 deficiency
-
primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
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|
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Saccharomyces cerevisiae S288C
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DOID:0111962
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combined immunodeficiency
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|
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Homo sapiens (human)
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|
DOID:0111961
|
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immunodeficiency 26
-
Aliases:
-
IMD26
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SCID due to DNA-PKcs deficiency
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immunodeficiency 26, with or without neurologic abnormalities
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severe combined immunodeficiency due to DNA-PKcs deficiency
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|
|
Homo sapiens (human)
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|
DOID:0111960
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immunodeficiency 15A
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Aliases:
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|
Mus musculus (house mouse)
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|
DOID:0111960
|
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immunodeficiency 15A
-
Aliases:
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Homo sapiens (human)
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|
DOID:0111959
|
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immunodeficiency 15B
-
Aliases:
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|
|
Mus musculus (house mouse)
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|
DOID:0111959
|
-
immunodeficiency 15B
-
Aliases:
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|
|
Homo sapiens (human)
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|
DOID:0111958
|
-
immunodeficiency 11B
-
Aliases:
-
IMD11B
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atopic dermatitis, elevated IgE, and eosinophilia
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immunodeficiency 11B with atopic dermatitis
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|
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Homo sapiens (human)
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|
DOID:0111957
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immunodeficiency 11A
-
Aliases:
-
CARD11 deficiency
-
IMD11A
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SCID due to CARD11 deficiency
-
severe combined immunodeficiency due to CARD11 deficiency
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|
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Homo sapiens (human)
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DOID:0111956
|
-
immunodeficiency 27B
-
Aliases:
-
IMD27B
-
autosomal dominant IFNGR1 deficiency
-
autosomal dominant MSMD due to partial IFNgammaR1 deficiency
-
autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency
-
autosomal dominant immunodeficiency 27B, mycobacteriosis
-
autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
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autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
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|
|
Homo sapiens (human)
|
|
DOID:0111956
|
-
immunodeficiency 27B
-
Aliases:
-
IMD27B
-
autosomal dominant IFNGR1 deficiency
-
autosomal dominant MSMD due to partial IFNgammaR1 deficiency
-
autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency
-
autosomal dominant immunodeficiency 27B, mycobacteriosis
-
autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
-
autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
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|
|
Mus musculus (house mouse)
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|
DOID:0111955
|
-
immunodeficiency 27A
-
Aliases:
-
IMD27A
-
autosomal recessive IFNGR1 deficiency
-
autosomal recessive MSMD due to partial IFNgammaR1 deficiency
-
autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency
-
autosomal recessive immunodeficiency 27A, mycobacteriosis
-
autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
-
autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
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|
|
Homo sapiens (human)
|
|
DOID:0111955
|
-
immunodeficiency 27A
-
Aliases:
-
IMD27A
-
autosomal recessive IFNGR1 deficiency
-
autosomal recessive MSMD due to partial IFNgammaR1 deficiency
-
autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency
-
autosomal recessive immunodeficiency 27A, mycobacteriosis
-
autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
-
autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
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|
|
Mus musculus (house mouse)
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|
DOID:0111954
|
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immunodeficiency 60
-
Aliases:
-
BACH2-related immunodeficiency and autoimmunity
-
BRIDA
-
IMD60
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|
|
Homo sapiens (human)
|
|
DOID:0111953
|
-
immunodeficiency 23
-
Aliases:
-
CID due to PGM3 deficiency
-
IMD23
-
PGM3-CDG
-
PGM3-related congenital disorder of glycosylation
-
combined immunodeficiency due to PGM3 deficiency
|
|
|
Saccharomyces cerevisiae S288C
|
|
DOID:0111953
|
-
immunodeficiency 23
-
Aliases:
-
CID due to PGM3 deficiency
-
IMD23
-
PGM3-CDG
-
PGM3-related congenital disorder of glycosylation
-
combined immunodeficiency due to PGM3 deficiency
|
|
|
Mus musculus (house mouse)
|
|
DOID:0111953
|
-
immunodeficiency 23
-
Aliases:
-
CID due to PGM3 deficiency
-
IMD23
-
PGM3-CDG
-
PGM3-related congenital disorder of glycosylation
-
combined immunodeficiency due to PGM3 deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:0111952
|
-
immunodeficiency 57
-
Aliases:
-
IMD57
-
immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome
-
immunodeficiency 57 with autoinflammation
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|
|
Homo sapiens (human)
|
|
DOID:0111951
|
-
immunodeficiency 40
-
Aliases:
|
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|
Mus musculus (house mouse)
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