DOID:8743
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erythema infectiosum
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Aliases:
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|
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Homo sapiens (human)
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DOID:0110164
|
-
Charcot-Marie-Tooth disease type 2D
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Aliases:
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CMT2D
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Charcot-Marie-Tooth disease neuronal type 2D
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Charcot-Marie-Tooth neuropathy type 2D
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autosomal dominant Charcot-Marie-Tooth disease type 2D
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|
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Homo sapiens (human)
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DOID:2536
|
-
chronic inflammatory demyelinating polyneuritis
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|
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Homo sapiens (human)
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DOID:0110031
|
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hemoglobin H disease
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Aliases:
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HBH
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alpha thalassemia, haemoglobin H type
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alpha thalassemia, hemoglobin H type
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alpha-thalassemia intermedia
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haemoglobin H disease
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haemoglobin H disease, deletional
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hemoglobin H disease, deletional
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|
|
Homo sapiens (human)
|
DOID:0060216
|
-
Cogan syndrome
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Aliases:
-
Cogan's syndrome
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diffuse interstitual keratitis
|
|
|
Homo sapiens (human)
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DOID:5509
|
|
|
|
Homo sapiens (human)
|
DOID:0110279
|
-
autosomal recessive limb-girdle muscular dystrophy type 2E
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Aliases:
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Beta-sarcoglycanopathy
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LGMD2E
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Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency
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muscular dystrophy, limb-girdle, type 2E
|
|
|
Homo sapiens (human)
|
DOID:4080
|
-
tricuspid valve insufficiency
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Aliases:
-
Tricuspid incompetence
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Tricuspid regurgitation
-
Tricuspid valve regurgitation
|
|
|
Homo sapiens (human)
|
DOID:0111071
|
-
congenital bile acid synthesis defect 1
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:1856
|
|
|
|
Homo sapiens (human)
|
DOID:2007
|
-
degeneration of macula and posterior pole
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Aliases:
-
degeneration of macula and posterior pole of retina
-
degeneration of macula or posterior pole
|
|
|
Homo sapiens (human)
|
DOID:0050883
|
-
infantile cerebellar-retinal degeneration
|
|
|
Homo sapiens (human)
|
DOID:10933
|
-
obsessive-compulsive disorder
-
Aliases:
-
Anancastic neurosis
-
obsessive compulsive disorder
|
|
|
Homo sapiens (human)
|
DOID:1474
|
-
aggressive periodontitis
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:10493
|
-
adrenal cortical hypofunction
-
Aliases:
-
Adrenal Cortical Insufficiency
-
Corticoadrenal insufficiency
|
|
|
Homo sapiens (human)
|
DOID:11661
|
-
blue color blindness
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:12145
|
-
detrusor sphincter dyssynergia
|
|
|
Homo sapiens (human)
|
DOID:2152
|
-
ovary epithelial cancer
-
Aliases:
-
Ovarian Surface epithelial-Stromal tumor
|
|
|
Homo sapiens (human)
|
DOID:10937
|
|
|
|
Homo sapiens (human)
|
DOID:0070127
|
-
congenital nongoitrous hypothyroidism 3
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110191
|
-
Charcot-Marie-Tooth disease type 4B1
-
Aliases:
-
CMT4B1
-
Charcot-Marie-Tooth neuropathy type 4B1
-
autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1
|
|
|
Homo sapiens (human)
|
DOID:2326
|
-
gastroenteritis
-
Aliases:
-
cholera morbus
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infectious colitis, enteritis and gastroenteritis
|
|
|
Homo sapiens (human)
|
DOID:615
|
|
|
|
Homo sapiens (human)
|
DOID:0081427
|
-
autosomal recessive distal hereditary motor neuronopathy 8
-
Aliases:
-
SORDD
-
sorbitol dehydrogenase deficiency with peripheral neuropathy
|
|
|
Homo sapiens (human)
|
DOID:0060699
|
-
familial hypocalciuric hypercalcemia
-
Aliases:
-
FBH
-
FBHH
-
FHH
-
familial benign hypercalcemia
-
familial benign hypocalciuric hypercalcemia
|
|
|
Homo sapiens (human)
|