Congenital hereditary muscular dystrophy

Congenital hereditary muscular dystrophy (disorder)

active

Code	`111501005`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20190731

Parents (2)

89886004Congenital anomaly of skeletal muscle disorder
193225000Hereditary progressive muscular dystrophy disorder

Children (37)

240075007Autosomal dominant muscular dystrophy not predominantly limb girdle disorder
240073000Autosomal recessive muscular dystrophy not predominantly limb girdle disorder
240055003Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein disorder
764812008Autosomal recessive myogenic arthrogryposis multiplex congenita disorder
718572004Bethlem myopathy disorder
725420009Congenital muscular dystrophy Paradas type disorder
771272007Congenital muscular dystrophy due to LMNA mutation disorder
787037000Congenital muscular dystrophy type 1A disorder
764944006Congenital muscular dystrophy type 1B disorder
890368007Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation disorder
890395002Congenital muscular dystrophy type 1D large gene mutation disorder
240061000Congenital muscular dystrophy with arthrogryposis multiplex congenita disorder
783176002Congenital muscular dystrophy with cerebellar involvement disorder
763314009Congenital muscular dystrophy with hyperlaxity disorder
715429006Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome disorder
771267003Congenital muscular dystrophy with integrin alpha-7 deficiency disorder
783174004Congenital muscular dystrophy with intellectual disability disorder
782772000Congenital muscular dystrophy with intellectual disability and severe epilepsy disorder
783175003Congenital muscular dystrophy without intellectual disability disorder
1172688004Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome disorder
55016009Congenital muscular hypertrophy-cerebral syndrome disorder
240104008Congenital myotonic dystrophy disorder
702343002Early onset myopathy with fatal cardiomyopathy disorder
240063002Eichsfeld type congenital muscular dystrophy disorder
723308003Epidermolysis bullosa simplex with muscular dystrophy disorder
240064008Hutterite type of muscular dystrophy disorder
1348306008Intermediate collagen VI-related muscular dystrophy disorder
1230273004Megaconial congenital muscular dystrophy disorder
111503008Merosin deficient congenital muscular dystrophy disorder
785298001Muscle eye brain disease with bilateral multicystic leukodystrophy disorder
111505001Muscle-eye-brain disease, congenital muscular dystrophy disorder
240058001Reunion-Indiana Amish type muscular dystrophy disorder
240062007Ullrich congenital muscular dystrophy disorder
111504002Walker-Warburg congenital muscular dystrophy disorder
240060004Western type of congenital muscular dystrophy disorder
240071003X-linked muscular dystrophy not predominantly limb girdle disorder
240047005X-linked muscular dystrophy with limb girdle distribution disorder