Congenital anomaly of skeletal muscle
Congenital anomaly of skeletal muscle
Hereditary progressive muscular dystrophy
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Congenital hereditary muscular dystrophy (disorder)
Congenital hereditary muscular dystrophy
congenitale musculaire dystrofie
CMD
Id111501005
StatusDefined
Associated morphologyDystrophy
Associated morphologyDystrophy
Finding siteSkeletal muscle structure
Finding siteSkeletal muscle structure
OccurrenceCongenital
Pathological processPathological developmental process
Clinical courseProgressive
PALGA thesaurus simple reference set for pathology
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG71.2
RuleTRUE
AdviceALWAYS G71.2
CorrelationSNOMED CT source code to target map code correlation not specified
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Autosomal dominant muscular dystrophy not predominantly limb girdle4
Autosomal recessive muscular dystrophy not predominantly limb girdle1
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein1
Autosomal recessive myogenic arthrogryposis multiplex congenita
Bethlem myopathy
Congenital muscular dystrophy due to LMNA mutation
Congenital muscular dystrophy Paradas type
Congenital muscular dystrophy type 1A
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation
Congenital muscular dystrophy type 1D large gene mutation
Congenital muscular dystrophy with arthrogryposis multiplex congenita
Congenital muscular dystrophy with cerebellar involvement
Congenital muscular dystrophy with hyperlaxity
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
Congenital muscular dystrophy with integrin alpha-7 deficiency
Congenital muscular dystrophy with intellectual disability
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Congenital muscular dystrophy without intellectual disability
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome
Congenital muscular hypertrophy-cerebral syndrome
Congenital myotonic dystrophy
Early onset myopathy with fatal cardiomyopathy
Eichsfeld type congenital muscular dystrophy
Epidermolysis bullosa simplex with muscular dystrophy
Hutterite type of muscular dystrophy
Megaconial congenital muscular dystrophy
Merosin deficient congenital muscular dystrophy
Muscle eye brain disease with bilateral multicystic leukodystrophy
Muscle-eye-brain disease, congenital muscular dystrophy
Reunion-Indiana Amish type muscular dystrophy
Ullrich congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy
Western type of congenital muscular dystrophy
X-linked muscular dystrophy not predominantly limb girdle
X-linked muscular dystrophy with limb girdle distribution2