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Symbol
Name
ID

Dmd
dystrophin, muscular dystrophy
MGI:94909

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Difficulty walking	Intellectual disability, mild	Obstructive sleep apnea	Hyporeflexia	Falls	Loss of ambulation	Tip-toe gait	Waddling gait	Delayed gross motor development
Disease(s) Associated with DMD	Difficulty walking	Intellectual disability, mild	Obstructive sleep apnea	Hyporeflexia	Falls	Loss of ambulation	Tip-toe gait	Waddling gait	Delayed gross motor development
Becker muscular dystrophy
Duchenne muscular dystrophy

Mouse Phenotypes		nervous system phenotype	abnormal corticotroph morphology	increased somatotroph cell size	abnormal Muller cell morphology	abnormal neuromuscular synapse morphology
Availability	Mouse Genotype	nervous system phenotype	abnormal corticotroph morphology	increased somatotroph cell size	abnormal Muller cell morphology	abnormal neuromuscular synapse morphology
	Dmd^mdx-3Cv/Dmd^mdx-3Cv
	Dmd^mdx/Dmd^mdx	*
	Dmd^mdx-3Cv/Y
	Dmd^mdx/Y	*

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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