congenital muscular dystrophy-dystroglycanopathy type A9

Summary
Synonym
  • MDDGA9
  • Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
  • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
Definition
A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.
Super Class
congenital muscular dystrophy-dystroglycanopathy type A
External Links
Disease Ontology
DOID:0111232
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1605 DAG1 dystroglycan 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
36773 Dg Dystroglycan
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q14118 Dystroglycan 1
The Human Phenotype Ontology
Displaying entries 51 - 60 of 69 in total
HPO ID HPO Term
HP:0001339 Lissencephaly
HP:0001460 Aplasia/Hypoplasia involving the skeletal musculature
HP:0002269 Abnormality of neuronal migration
HP:0002334 Abnormal cerebellar vermis morphology
HP:0002536 Abnormal cortical gyration
HP:0003202 Skeletal muscle atrophy
HP:0003560 Muscular dystrophy
HP:0007731 Chorioretinal dysplasia
HP:0007957 Corneal opacity
HP:0007973 Retinal dysplasia
Displaying entries 1 - 10 of 13 in total
Gene ID Gene Symbol Description
1605 DAG1 dystroglycan 1
10329 RXYLT1 ribitol xylosyltransferase 1
10585 POMT1 protein O-mannosyltransferase 1
11041 B4GAT1 beta-1,4-glucuronyltransferase 1
148789 B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
2218 FKTN fukutin
29954 POMT2 protein O-mannosyltransferase 2
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
729920 CRPPA CDP-L-ribitol pyrophosphorylase A
79147 FKRP fukutin related protein

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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: August 19, 2024