DOID:8503
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Homo sapiens (human)
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DOID:10488
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imperforate anus
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Aliases:
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Congenital atresia of anus
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Congenital or infantile occlusion of anus
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anal atresia
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Homo sapiens (human)
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DOID:0060025
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immunoglobulin alpha deficiency
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Aliases:
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IgA deficiency
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gamma-A-globulin deficiency
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Homo sapiens (human)
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DOID:0060758
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immunodeficiency with hyper-IgM type 2
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Aliases:
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AID deficiency
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HIGM2
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activation-induced cytidine deaminase deficiency
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hyper-IgM syndrome type 2
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Homo sapiens (human)
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DOID:0060759
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immunodeficiency with hyper IgM type 5
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Aliases:
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HIGM5
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hyper-IgM syndrome 5
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hyper-IgM syndrome due to UNG deficiency
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hyper-IgM syndrome due to uracil N-glycosylase
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Mus musculus (house mouse)
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DOID:0060759
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immunodeficiency with hyper IgM type 5
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Aliases:
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HIGM5
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hyper-IgM syndrome 5
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hyper-IgM syndrome due to UNG deficiency
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hyper-IgM syndrome due to uracil N-glycosylase
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Homo sapiens (human)
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DOID:0060759
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immunodeficiency with hyper IgM type 5
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Aliases:
-
HIGM5
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hyper-IgM syndrome 5
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hyper-IgM syndrome due to UNG deficiency
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hyper-IgM syndrome due to uracil N-glycosylase
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Saccharomyces cerevisiae S288C
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DOID:0060759
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immunodeficiency with hyper IgM type 5
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Aliases:
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HIGM5
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hyper-IgM syndrome 5
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hyper-IgM syndrome due to UNG deficiency
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hyper-IgM syndrome due to uracil N-glycosylase
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Caenorhabditis elegans
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DOID:0060023
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immunodeficiency with hyper IgM type 3
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Aliases:
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CD40 deficiency
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HIGM3
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hyper-IgM syndrome due to CD40 deficiency
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type 3 hyper-IgM immunodeficiency
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Homo sapiens (human)
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DOID:0112002
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immunodeficiency 47
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Aliases:
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CDG IIs
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CDG2S
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CDGIIs
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IMD47
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congenital disorder of glycosylation type IIs
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immunodeficiency and hepatopathy with or without neurologic features
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|
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Homo sapiens (human)
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DOID:0111949
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immunodeficiency 36
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Aliases:
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IMD36
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activated phosphoinositide 3-kinase delta syndrome 2
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|
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Mus musculus (house mouse)
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DOID:0111949
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immunodeficiency 36
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Aliases:
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IMD36
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activated phosphoinositide 3-kinase delta syndrome 2
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Rattus norvegicus (Norway rat)
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DOID:0111953
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immunodeficiency 23
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Aliases:
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CID due to PGM3 deficiency
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IMD23
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PGM3-CDG
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PGM3-related congenital disorder of glycosylation
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combined immunodeficiency due to PGM3 deficiency
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|
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Homo sapiens (human)
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DOID:0111953
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immunodeficiency 23
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Aliases:
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CID due to PGM3 deficiency
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IMD23
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PGM3-CDG
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PGM3-related congenital disorder of glycosylation
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combined immunodeficiency due to PGM3 deficiency
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|
|
Saccharomyces cerevisiae S288C
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DOID:0111953
|
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immunodeficiency 23
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Aliases:
-
CID due to PGM3 deficiency
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IMD23
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PGM3-CDG
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PGM3-related congenital disorder of glycosylation
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combined immunodeficiency due to PGM3 deficiency
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|
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Mus musculus (house mouse)
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DOID:0111936
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immunodeficiency 14
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Aliases:
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APDS
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IMD14
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PASLI disease
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activated PI3K-delta syndrome
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senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation
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Homo sapiens (human)
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DOID:4784
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immune-complex glomerulonephritis
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Aliases:
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Immune Complex Glomerulonephritis
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Homo sapiens (human)
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DOID:2914
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|
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Homo sapiens (human)
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DOID:0090110
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immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
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Aliases:
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Autoimmune enteropathy type 1
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DMSD
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IDDM-secretory diarrhea syndrome
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IPEX
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X-linked autoimmunity-allergic dysregulation syndrome
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XLAAD
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XPID
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autoimmunity-immunodeficiency syndrome, X-linked
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diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea
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diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked
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immunodeficiency, polyendocrinopathy, and enteropathy, X-linked
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immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked
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Homo sapiens (human)
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DOID:8440
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Homo sapiens (human)
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DOID:0060190
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Homo sapiens (human)
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DOID:0060189
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Drosophila melanogaster (fruit fly)
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DOID:0060189
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|
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Rattus norvegicus (Norway rat)
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DOID:0060189
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|
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Homo sapiens (human)
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DOID:0060189
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|
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Mus musculus (house mouse)
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