Human Disease and Mouse Model Detail
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Human Disease
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Muscular Dystrophy-Dystroglycanopathy (congenital without Mental Retardation), Type B, 4; MDDGB4
OMIM ID: 613152
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Synonyms
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Muscular Dystrophy, Congenital, Fktn-Related
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Fktn*
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FKTN*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Muscular Dystrophy-Dystroglycanopathy (congenital without Mental Retardation), Type B, 4; MDDGB4
Associated Mouse Gene:
Fktn
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