DOID:438
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-
autoimmune disease of the nervous system
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|
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Homo sapiens (human)
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DOID:417
|
-
autoimmune disease
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Aliases:
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autoimmune hypersensitivity disease
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hypersensitivity reaction type II disease
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|
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Homo sapiens (human)
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DOID:718
|
-
autoimmune hemolytic anemia
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Aliases:
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Autoimmune haemolytic anaemia
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autoimmune hemolytic anaemia
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|
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Homo sapiens (human)
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DOID:2048
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-
autoimmune hepatitis
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Aliases:
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Autoimmune chronic active hepatitis
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autoimmune hepatitis with centrilobular necrosis
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|
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Homo sapiens (human)
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DOID:0110115
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-
autoimmune lymphoproliferative syndrome type 2A
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Aliases:
-
ALPS2A
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autoimmune lymphoproliferative syndrome type IIA
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|
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Homo sapiens (human)
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DOID:0110116
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-
autoimmune lymphoproliferative syndrome type 2B
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Aliases:
-
ALPS with recurrent viral infections
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ALPS2B
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CEDS
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Caspase 8 deficiency
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Caspase 8 deficiency syndrome
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Caspase eight deficiency state
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autoimmune lymphoproliferative syndrome type IIB
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autoimmune lymphoproliferative syndrome with recurrent viral infections
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|
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Homo sapiens (human)
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DOID:0110119
|
-
autoimmune lymphoproliferative syndrome type 3
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Aliases:
-
ALPS3
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autoimmune lymphoproliferative syndrome type III
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|
|
Homo sapiens (human)
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DOID:6688
|
-
autoimmune lymphoproliferative syndrome
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Aliases:
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ALPS
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Canale-Smith syndrome
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|
|
Homo sapiens (human)
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DOID:0040091
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|
|
|
Homo sapiens (human)
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DOID:0050167
|
-
autoimmune polyendocrine syndrome type 1
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Aliases:
-
Autoimmune Polyglandular Syndrome I
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Whitaker syndrome
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autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
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|
|
Homo sapiens (human)
|
DOID:14040
|
-
autoimmune polyendocrine syndrome
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Aliases:
-
Autoimmune polyglandular failure
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Lloyd's syndrome
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autoimmune polyendocrinopathy
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|
|
Homo sapiens (human)
|
DOID:8924
|
-
autoimmune thrombocytopenic purpura
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Aliases:
-
Immune thrombocytopenic purpura
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idiopathic thrombocytopenic purpura
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primary thrombocytopenic purpura
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|
|
Homo sapiens (human)
|
DOID:7188
|
-
autoimmune thyroiditis
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Aliases:
-
Chronic Lymphocytic Thyroiditis
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Hashimoto thyroiditis
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Hashimoto's Disease
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Hashimoto's syndrome
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Hashimoto's thyroiditis
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Lymphocytic Thyroiditis
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|
|
Homo sapiens (human)
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DOID:11504
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|
|
|
Homo sapiens (human)
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DOID:0070247
|
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autosomal dominant Emery-Dreifuss muscular dystrophy 2
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Aliases:
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EDMD2
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EMD2
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Emery-Dreifuss muscular dystrophy 2, autosomal dominant
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Emery-Dreifuss muscular dystrophy, autosomal dominant
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Hauptmann-Thannhauser muscular dystrophy
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autosomal dominant limb-girdle muscular dystrophy type 1B
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muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
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scapuloilioperoneal atrophy with cardiopathy
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|
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Homo sapiens (human)
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DOID:0060766
|
-
autosomal dominant Robinow syndrome 1
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0060765
|
-
autosomal dominant Robinow syndrome 2
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0060767
|
-
autosomal dominant Robinow syndrome 3
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0060690
|
-
autosomal dominant auditory neuropathy 1
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Aliases:
-
AUNA1
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NSDAN
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nonsyndromic dominant auditory neuropathy
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|
|
Homo sapiens (human)
|
DOID:0111217
|
-
autosomal dominant centronuclear myopathy
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:1441
|
-
autosomal dominant cerebellar ataxia
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0060293
|
-
autosomal dominant chondrodysplasia punctata
|
|
|
Homo sapiens (human)
|
DOID:0070130
|
-
autosomal dominant cutis laxa 1
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0070136
|
-
autosomal dominant cutis laxa 2
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0070131
|
-
autosomal dominant cutis laxa 3
-
Aliases:
|
|
|
Homo sapiens (human)
|