DOID:0110292
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autosomal recessive limb-girdle muscular dystrophy type 2O
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Aliases:
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LGMD2O
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MDDGC3
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C3
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muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related
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Homo sapiens (human)
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DOID:0110293
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autosomal recessive limb-girdle muscular dystrophy type 2P
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Aliases:
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LGMD2P
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MDDGC9
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
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muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
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Homo sapiens (human)
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DOID:0110285
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autosomal recessive limb-girdle muscular dystrophy type 2Q
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Aliases:
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LGMD2Q
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autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency
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muscular dystrophy, limb-girdle, type 2Q
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Homo sapiens (human)
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DOID:0110287
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autosomal recessive limb-girdle muscular dystrophy type 2S
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Aliases:
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LGMD2S
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muscular dystrophy, limb-girdle, type 2S
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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: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:0110289
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autosomal recessive limb-girdle muscular dystrophy type 2Y
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Aliases:
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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)
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DOID:0080762
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autosomal recessive limb-girdle muscular dystrophy type 2Z
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Aliases:
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limb-girdle muscular dystrophy 21
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Homo sapiens (human)
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DOID:0110274
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autosomal recessive limb-girdle muscular dystrophy
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Homo sapiens (human)
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DOID:0110462
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autosomal recessive nonsyndromic deafness 101
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Aliases:
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DFNB101
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autosomal recessive deafness 101
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Homo sapiens (human)
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DOID:0110463
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autosomal recessive nonsyndromic deafness 102
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Aliases:
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DFNB102
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autosomal recessive deafness 102
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Homo sapiens (human)
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DOID:0110464
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autosomal recessive nonsyndromic deafness 103
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Aliases:
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DFNB103
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autosomal recessive deafness 103
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Homo sapiens (human)
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DOID:0110465
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autosomal recessive nonsyndromic deafness 104
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Aliases:
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DFNB104
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autosomal recessive deafness 104
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Homo sapiens (human)
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DOID:0110467
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autosomal recessive nonsyndromic deafness 12
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Aliases:
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DFNB12
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autosomal recessive deafness 12
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Homo sapiens (human)
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DOID:0110468
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autosomal recessive nonsyndromic deafness 13
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Aliases:
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DFNB13
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autosomal recessive deafness 13
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Homo sapiens (human)
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DOID:0110469
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autosomal recessive nonsyndromic deafness 14
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Aliases:
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DFNB14
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autosomal recessive deafness 14
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Homo sapiens (human)
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DOID:0110470
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autosomal recessive nonsyndromic deafness 15
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Aliases:
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DFNB15
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DFNB72
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DFNB95
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autosomal recessive deafness 15
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autosomal recessive deafness 72
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autosomal recessive deafness 95
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Homo sapiens (human)
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DOID:0110471
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autosomal recessive nonsyndromic deafness 16
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Aliases:
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DFNB16
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autosomal recessive deafness 16
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Homo sapiens (human)
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DOID:0110472
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autosomal recessive nonsyndromic deafness 17
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Aliases:
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DFNB17
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autosomal recessive deafness 17
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Homo sapiens (human)
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DOID:0110473
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autosomal recessive nonsyndromic deafness 18A
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Aliases:
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DFNB18A
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autosomal recessive deafness 18A
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Homo sapiens (human)
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DOID:0110474
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autosomal recessive nonsyndromic deafness 18B
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Aliases:
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DFNB18B
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autosomal recessive deafness 18B
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Homo sapiens (human)
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DOID:0110475
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autosomal recessive nonsyndromic deafness 1A
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Aliases:
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DFNB1A
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autosomal recessive deafness 1A
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Homo sapiens (human)
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DOID:0110476
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autosomal recessive nonsyndromic deafness 1B
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Aliases:
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DFNB1B
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autosomal recessive deafness 1B
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Homo sapiens (human)
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DOID:0110477
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autosomal recessive nonsyndromic deafness 2
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Aliases:
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DFNB2
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autosomal recessive deafness 2
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Homo sapiens (human)
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DOID:0110478
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autosomal recessive nonsyndromic deafness 20
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Aliases:
-
DFNB20
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autosomal recessive deafness 20
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Homo sapiens (human)
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