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8C70.6 Congenital muscular dystrophy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Congenital muscular dystrophies with central nervous system abnormalities are a heterogeneous group of autosomal recessively inherited degenerative muscle disorders associated with cerebral and cerebellar dysplasia, white matter abnormalities and ocular abnormalities in some subtypes.

postcoordination

synonyms

• Congenital muscular dystrophy
• hereditary muscular dystrophy
• congenital hereditary muscular dystrophy
• congenital progressive muscular dystrophy
• hereditary progressive muscular dystrophy
• Congenital muscular dystrophy with central nervous system abnormalities
• Congenital muscular dystrophy Fukuyama type
• Congenital muscular dystrophy with central nervous system abnormalities, not elsewhere classified
• Walker Warburg syndrome
• Hydrocephalus - agyria - retinal dysplasia syndrome
• WWS - [Walker Warburg syndrome]
• HARD - [Hydrocephalus - agyria - retinal dysplasia syndrome]
• Muscle Eye Brain disease
• MEB - [Muscle Eye Brain disease]
• Marinesco-Sjögren syndrome
• Congenital muscular dystrophy type 1C, fukutin-related protein gene mutation
• Congenital muscular dystrophy type 1D large gene mutation
• MDC1D - [congenital muscular dystrophy 1D]
• Congenital muscular dystrophy without central nervous system symptoms
• Congenital muscular dystrophy without central nervous system abnormalities, not elsewhere classified
• Merosin or laminin alpha 2 chain deficiency
• Merosin-deficient congenital muscular dystrophy
• Collagen VI deficiency
• Bethlem myopathy
• Ullrich congenital muscular dystrophy
• UCMD - [Ullrich congenital muscular dystrophy
• Congenital muscular dystrophy - infantile cataract - hypogonadism
• Bassoe syndrome
• Congenital muscular dystrophy due to lamin A/C deficiency
• Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect
• Congenital megaconial myopathy
• Congenital muscular dystrophy with mitochondrial structural abnormalities
• Congenital muscular dystrophy with integrin deficiency
• Congenital muscular dystrophy, Paradas type
• Rigid spine syndrome
• Congenital muscular dystrophy type 1B
• MDC1B - [

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