DOID:65
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connective tissue disease
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Aliases:
-
connective tissue disorder
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disorder of connective tissue
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Homo sapiens (human)
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DOID:8866
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actinic keratosis
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Aliases:
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SK - Solar keratosis
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Senile hyperkeratosis
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Solar keratosis
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actinic (Solar) Keratosis
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Homo sapiens (human)
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DOID:12030
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Homo sapiens (human)
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DOID:240
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|
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Homo sapiens (human)
|
DOID:4353
|
|
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Homo sapiens (human)
|
DOID:13141
|
|
|
|
Homo sapiens (human)
|
DOID:1283
|
|
|
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Homo sapiens (human)
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DOID:0050742
|
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nicotine dependence
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Aliases:
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Homo sapiens (human)
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DOID:0110304
|
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autosomal dominant limb-girdle muscular dystrophy type 2
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Aliases:
-
LGMD1F
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autosomal dominant limb-girdle muscular dystrophy type 1F
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muscular dystrophy limb-girdle type 1F
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Homo sapiens (human)
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DOID:0110302
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obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
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|
Homo sapiens (human)
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DOID:0110295
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autosomal recessive limb-girdle muscular dystrophy type 2U
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Aliases:
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LGMD2U
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MDDGC7
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autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency
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muscular dystrophy limb-girdle type 2U
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C7
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|
|
Homo sapiens (human)
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DOID:0110284
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autosomal recessive limb-girdle muscular dystrophy type 2L
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Aliases:
-
LGMD2L
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muscular dystrophy, limb-girdle, type 2L
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|
|
Homo sapiens (human)
|
DOID:0110289
|
-
autosomal recessive limb-girdle muscular dystrophy type 2Y
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Aliases:
-
LGMD2Y
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autosomal recessive muscular dystrophy due to LAP1B deficiency
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autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency
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muscular dystrophy with progressive weakness, distal contractures and rigid spine
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muscular dystrophy, limb-girdle, type 2Y
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|
|
Homo sapiens (human)
|
DOID:0110299
|
-
autosomal recessive limb-girdle muscular dystrophy type 2I
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Aliases:
-
LGMD2I
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Limb-girdle muscular dystrophy due to FKRP deficiency
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MDDGC5
-
muscular dystrophy limb-girdle type 2I
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
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muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
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|
|
Homo sapiens (human)
|
DOID:0110287
|
-
autosomal recessive limb-girdle muscular dystrophy type 2S
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Aliases:
-
LGMD2S
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muscular dystrophy, limb-girdle, type 2S
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|
|
Homo sapiens (human)
|
DOID:0110278
|
-
autosomal recessive limb-girdle muscular dystrophy type 2D
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Aliases:
-
Alpha-sarcoglycanopathy
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DMDA2
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Duchenne-like autosomal recessive muscular dystrophy type 2
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LGMD2D
-
muscular dystrophy, limb-girdle, type 2D
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primary adhalinopathy
|
|
|
Homo sapiens (human)
|
DOID:0110292
|
-
autosomal recessive limb-girdle muscular dystrophy type 2O
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Aliases:
-
LGMD2O
-
MDDGC3
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C3
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muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related
|
|
|
Homo sapiens (human)
|
DOID:0110294
|
-
autosomal recessive limb-girdle muscular dystrophy type 2T
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Aliases:
-
LGMD2T
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MDDGC14
-
muscular dystrophy limb-girdle type 2T
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C14
-
muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related
|
|
|
Homo sapiens (human)
|
DOID:0110301
|
-
obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
|
|
|
Homo sapiens (human)
|
DOID:0110300
|
-
obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
|
|
|
Homo sapiens (human)
|
DOID:0110293
|
-
autosomal recessive limb-girdle muscular dystrophy type 2P
-
Aliases:
-
LGMD2P
-
MDDGC9
-
muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
-
muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
|
|
|
Homo sapiens (human)
|
DOID:0110281
|
-
autosomal recessive limb-girdle muscular dystrophy type 2G
-
Aliases:
-
LGMD2G
-
limb-girdle muscular dystrophy due to telethonin deficiency
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muscular dystrophy, limb-girdle, type 2G
|
|
|
Homo sapiens (human)
|
DOID:0110306
|
-
autosomal dominant limb-girdle muscular dystrophy type 3
-
Aliases:
-
LGMD1G
-
autosomal dominant limb-girdle muscular dystrophy type 1G
-
muscular dystrophy limb-girdle type 1G
|
|
|
Homo sapiens (human)
|
DOID:0110279
|
-
autosomal recessive limb-girdle muscular dystrophy type 2E
-
Aliases:
-
Beta-sarcoglycanopathy
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LGMD2E
-
Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency
-
muscular dystrophy, limb-girdle, type 2E
|
|
|
Homo sapiens (human)
|
DOID:0110297
|
-
autosomal recessive limb-girdle muscular dystrophy type 2K
-
Aliases:
-
LGMD2K
-
MDDGC1
-
limb-girdle muscular dystrophy-intellectual disability syndrome
-
muscular dystrophy limb-girdle type 2K
-
muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1
|
|
|
Homo sapiens (human)
|