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
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Laterality - only one may be selected
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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