Concept information
Preferred term
Congenital hereditary muscular dystrophy
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder)
- Bethlem myopathy (disorder)
- Congenita hypotonic - sclerotic muscular dystrophy
- Congenital muscular dystrophy due to lamin A/C mutation
- Congenital muscular dystrophy Paradas type (disorder)
- Congenital muscular dystrophy type 1B
- Congenital muscular dystrophy with arthrogryposis multiplex congenita
- Congenital muscular dystrophy with cerebellar involvement
- Congenital muscular dystrophy with hyperlaxity (disorder)
- Congenital muscular dystrophy with integrin alpha-7 deficiency (disorder)
- Congenital muscular dystrophy with intellectual disability
- Congenital muscular dystrophy with intellectual disability and severe epilepsy
- Congenital muscular dystrophy without intellectual disability (disorder)
- Congenital muscular hypertrophy-cerebral syndrome
- Eichsfeld type congenital muscular dystrophy
- Epidermolysis bullosa simplex with muscular dystrophy (disorder)
- Merosin-negative congenital muscular dystrophy
- Muscle eye brain disease with bilateral multicystic leucodystrophy
- Reunion-Indiana Amish type muscular dystrophy
- Salih congenital muscular dystrophy
- Western type of congenital muscular dystrophy
Associated morphology
Clinical course
Finding site
Is a
- 193225000
- Congenital anomaly of skeletal muscle
Occurrence
Pathological process
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/111501005
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