muscular dystrophy-dystroglycanopathy type B6

Summary
Synonym
  • MDC1D
  • MDDGB6
  • congenital muscular dystrophy LARGE-related
  • congenital muscular dystrophy type 1D
  • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
  • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
Definition
A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with mental retardation and structural brain abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LARGE gene on chromosome 22q12.
Super Class
autosomal recessive disease muscular dystrophy-dystroglycanopathy type B
Disease Ontology
DOID:0110637
ORDO
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9215 LARGE1 LARGE xylosyl- and glucuronyltransferase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
16795 Large1 LARGE xylosyl- and glucuronyltransferase 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
D9IG22 LARGE-1 (Fragment)
The Human Phenotype Ontology
Displaying entries 11 - 20 of 60 in total
HPO ID HPO Term
HP:0003236 Elevated circulating creatine kinase concentration
HP:0001263 Global developmental delay
HP:0008443 Neuropathic spinal arthropathy
HP:0002120 Cerebral cortical atrophy
HP:0010864 Intellectual disability, severe
HP:0001321 Cerebellar hypoplasia
HP:0003712 Skeletal muscle hypertrophy
HP:0000545 Myopia
HP:0002650 Scoliosis
HP:0000028 Cryptorchidism
Displaying all 5 entries
Gene ID Gene Symbol Description
10585 POMT1 protein O-mannosyltransferase 1
29925 GMPPB GDP-mannose pyrophosphorylase B
29954 POMT2 protein O-mannosyltransferase 2
79147 FKRP fukutin related protein
9215 LARGE1 LARGE xylosyl- and glucuronyltransferase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026