|
Symbol Name ID |
Idua
iduronidase, alpha-L MGI:96418 |
| Darker colors indicate more annotations |
| Human Phenotypes | Spastic paraparesis |
Abnormal CNS myelination |
Hydrocephalus |
Cervical cord compression |
Neurodegeneration |
Cerebral palsy |
Abnormal pyramidal sign |
Abnormal nerve conduction velocity |
Depression |
Progressive neurologic deterioration |
Intellectual disability |
Sleep abnormality |
Obstructive sleep apnea |
Global developmental delay |
Constrictive median neuropathy |
| 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 |
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| 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) |
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last database update 04/23/2024 MGI 6.23 |
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