Symbol Name ID |
Idua
iduronidase, alpha-L MGI:96418 |
Darker colors indicate more annotations |
Human Phenotypes | Spastic paraparesis |
Hydrocephalus |
Cerebral palsy |
Abnormal pyramidal sign |
Abnormal nerve conduction velocity |
Depression |
Intellectual disability |
Sleep abnormality |
Global developmental delay |
Disease(s) Associated with IDUA | |||||||||
mucopolysaccharidosis Ih | |||||||||
mucopolysaccharidosis Ih/s | |||||||||
Scheie syndrome |
Mouse Phenotypes | cochlear hair cell degeneration |
abnormal microglial cell morphology |
abnormal microglial cell physiology |
abnormal cerebellar cortex morphology |
abnormal Purkinje cell morphology |
Purkinje cell degeneration |
abnormal neuron morphology |
cochlear ganglion degeneration |
|
Availability | Mouse Genotype | ||||||||
Iduatm1Clk/Iduatm1Clk | |||||||||
Iduatm1Efn/Iduatm1Efn |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 07/02/2024 MGI 6.13 |
![]() |
|