DOID:0110296
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autosomal recessive limb-girdle muscular dystrophy type 2M
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Aliases:
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LGMD2M
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MDDGC4
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4
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Homo sapiens (human)
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DOID:0110286
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obsolete autosomal recessive limb-girdle muscular dystrophy type 2R
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Homo sapiens (human)
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DOID:0110278
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autosomal recessive limb-girdle muscular dystrophy type 2D
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Aliases:
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Alpha-sarcoglycanopathy
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DMDA2
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Duchenne-like autosomal recessive muscular dystrophy type 2
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LGMD2D
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muscular dystrophy, limb-girdle, type 2D
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primary adhalinopathy
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Homo sapiens (human)
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DOID:0110294
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autosomal recessive limb-girdle muscular dystrophy type 2T
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Aliases:
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LGMD2T
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MDDGC14
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muscular dystrophy limb-girdle type 2T
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C14
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muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related
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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:
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LGMD2L
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muscular dystrophy, limb-girdle, type 2L
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Homo sapiens (human)
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DOID:11727
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facioscapulohumeral muscular dystrophy
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Aliases:
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Landouzy Dejerine muscular dystrophy
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Landouzy-Dejerine muscular dystrophy
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Muscular dystrophy, Landouzy-Dejerine
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Homo sapiens (human)
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DOID:0110281
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autosomal recessive limb-girdle muscular dystrophy type 2G
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Aliases:
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LGMD2G
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limb-girdle muscular dystrophy due to telethonin deficiency
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muscular dystrophy, limb-girdle, type 2G
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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:
-
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:0110306
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autosomal dominant limb-girdle muscular dystrophy type 3
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Aliases:
-
LGMD1G
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autosomal dominant limb-girdle muscular dystrophy type 1G
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muscular dystrophy limb-girdle type 1G
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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:0110300
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obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
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|
|
Homo sapiens (human)
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DOID:0110273
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autosomal dominant limb-girdle muscular dystrophy
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|
|
Homo sapiens (human)
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DOID:0110301
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obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
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|
Homo sapiens (human)
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DOID:1307
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|
|
|
Homo sapiens (human)
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DOID:1588
|
|
|
|
Homo sapiens (human)
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DOID:3659
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|
|
|
Homo sapiens (human)
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DOID:5408
|
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Paget's disease of bone
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Aliases:
-
Paget disease of bone
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Paget's bone disease
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osseous Paget's disease
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osteitis deformans
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|
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Homo sapiens (human)
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DOID:0060672
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Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
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Homo sapiens (human)
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DOID:9255
|
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frontotemporal dementia
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Aliases:
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Wilhemsen-Lynch disease
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frontotemporal lobar degeneration
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multiple system tauopathy with presenile dementia
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pallidopontonigral degeneration
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|
|
Homo sapiens (human)
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DOID:440
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|
|
|
Homo sapiens (human)
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DOID:0111338
|
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isolated elevated serum creatine phosphokinase levels
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Aliases:
-
elevated serum CPK
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idiopathic hyperCKemia
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isolated hyperCKemia
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|
|
Homo sapiens (human)
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DOID:12506
|
-
Bell's palsy
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Aliases:
-
Bell palsy
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Bell's (facial) palsy
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|
|
Homo sapiens (human)
|
DOID:13934
|
-
facial paralysis
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:1756
|
|
|
|
Homo sapiens (human)
|
DOID:633
|
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myositis
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Aliases:
-
Inflammatory disorder of muscle
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|
|
Homo sapiens (human)
|