Concept information
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Musculoskeletal system finding
Disease of the musculoskeletal system, NOS
Disorder of muscle
Congenital anomaly of skeletal muscle
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Disorder of body system
Disease of the musculoskeletal system, NOS
Disorder of muscle
Congenital anomaly of skeletal muscle
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General finding of soft tissue
Disorder of soft tissue
Disorder of muscle
Congenital anomaly of skeletal muscle
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Disorder of muscle
Disorder of muscle
muscular dystrophy
Hereditary progressive muscular dystrophy
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Disorder of muscle
Disorder of muscle
muscular dystrophy
Hereditary progressive muscular dystrophy
...
Disease of the musculoskeletal system, NOS
Disorder of muscle
muscular dystrophy
Hereditary progressive muscular dystrophy
...
Disease of the musculoskeletal system, NOS
Disorder of muscle
muscular dystrophy
Hereditary progressive muscular dystrophy
...
Disorder of soft tissue
Disorder of muscle
muscular dystrophy
Hereditary progressive muscular dystrophy
...
Disorder of soft tissue
Disorder of muscle
muscular dystrophy
Hereditary progressive muscular dystrophy
Preferred term
Congenital hereditary muscular dystrophy
Type
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http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Narrower concepts
- Autosomal dominant muscular dystrophy not predominantly limb girdle
- Autosomal recessive muscular dystrophy not predominantly limb girdle
- Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
- Hutterite type of muscular dystrophy
- Merosin deficient congenital muscular dystrophy
- Muscle-eye-brain disease, congenital muscular dystrophy
- Walker-Warburg congenital muscular dystrophy
- X-linked muscular dystrophy not predominantly limb girdle
- X-linked muscular dystrophy with limb girdle distribution
Associated morphology
Clinical course
Finding site
Occurrence
Pathological process
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/111501005
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