DOID:0110256
|
-
cataract 21 multiple types
-
Aliases:
-
CTRCT21
-
cataract 21 multiple types with or without microcornea
|
|
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Homo sapiens (human)
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DOID:0110257
|
|
|
|
Homo sapiens (human)
|
DOID:0110258
|
-
cataract 10 multiple types
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110259
|
|
|
|
Homo sapiens (human)
|
DOID:0110260
|
|
|
|
Homo sapiens (human)
|
DOID:0110261
|
-
cataract 35
-
Aliases:
-
CATCN1
-
CTRCT35
-
autosomal recessive congenital nuclear cataract 1
-
cataract 35, congenital nuclear
|
|
|
Homo sapiens (human)
|
DOID:0110262
|
|
|
|
Homo sapiens (human)
|
DOID:0110263
|
-
cataract 19 multiple types
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110264
|
|
|
|
Homo sapiens (human)
|
DOID:0110265
|
-
cataract 31 multiple types
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110266
|
-
cataract 9 multiple types
-
Aliases:
-
CTRCT9
-
cataract 9 multiple types with or without microcornea
|
|
|
Homo sapiens (human)
|
DOID:0110267
|
-
cataract 44
-
Aliases:
-
CTRCT44
-
total early-onset cataract
|
|
|
Homo sapiens (human)
|
DOID:0110268
|
-
cataract 22 multiple types
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110269
|
-
cataract 3 multiple types
-
Aliases:
-
CTRCT3
-
cataract 3 multiple types with or without microcornea
|
|
|
Homo sapiens (human)
|
DOID:0110270
|
-
cataract 17 multiple types
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110271
|
-
cataract 23
-
Aliases:
-
CTRCT23
-
lamellar cataract 23
|
|
|
Homo sapiens (human)
|
DOID:0110272
|
-
cataract 40
-
Aliases:
-
CTRCT40
-
cataract 40 X-linked
-
cataract 40 with or without microcornea
|
|
|
Homo sapiens (human)
|
DOID:0110273
|
-
autosomal dominant limb-girdle muscular dystrophy
|
|
|
Homo sapiens (human)
|
DOID:0110274
|
-
autosomal recessive limb-girdle muscular dystrophy
|
|
|
Homo sapiens (human)
|
DOID:0110275
|
-
autosomal recessive limb-girdle muscular dystrophy type 2A
-
Aliases:
-
LGMD2A
-
Leyden-Moebius muscular dystrophy
-
limb-girdle muscular dystrophy due to calpain deficiency
-
muscular dystrophy, limb-girdle, type 2A
-
pelvofemoral muscular dystrophy
-
primary calpainopathy
|
|
|
Homo sapiens (human)
|
DOID:0110276
|
-
autosomal recessive limb-girdle muscular dystrophy type 2B
-
Aliases:
-
LGMD2B
-
LGMD3
-
limb-girdle muscular dystrophy due to dysferlin deficiency
-
limb-girdle muscular dystrophy type 3
|
|
|
Homo sapiens (human)
|
DOID:0110277
|
-
autosomal recessive limb-girdle muscular dystrophy type 2C
-
Aliases:
-
DMDA1
-
LGMD2C
-
Maghrebian myopathy
-
SCARMD
-
autosomal recessive Duchenne-like muscular dystrophy type 1
-
deficiency of sarcoglycan gamma
-
gamma-sarcoglycanopathy
-
limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency
-
muscular dystrophy, limb-girdle, type 2C
-
severe childhood autosomal recessive muscular dystrophy North African type
|
|
|
Homo sapiens (human)
|
DOID:0110278
|
-
autosomal recessive limb-girdle muscular dystrophy type 2D
-
Aliases:
-
Alpha-sarcoglycanopathy
-
DMDA2
-
Duchenne-like autosomal recessive muscular dystrophy type 2
-
LGMD2D
-
muscular dystrophy, limb-girdle, type 2D
-
primary adhalinopathy
|
|
|
Homo sapiens (human)
|
DOID:0110279
|
-
autosomal recessive limb-girdle muscular dystrophy type 2E
-
Aliases:
-
Beta-sarcoglycanopathy
-
LGMD2E
-
Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency
-
muscular dystrophy, limb-girdle, type 2E
|
|
|
Homo sapiens (human)
|
DOID:0110280
|
-
autosomal recessive limb-girdle muscular dystrophy type 2F
-
Aliases:
-
LGMD2F
-
delta-sarcoglycanopathy
-
limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency
|
|
|
Homo sapiens (human)
|