|
Symbol Name ID |
Gcdh
glutaryl-Coenzyme A dehydrogenase MGI:104541 |
| Darker colors indicate more annotations |
| Human Phenotypes | Subdural hemorrhage |
Dysphagia |
Spastic diplegia |
Opisthotonus |
Symmetrical progressive peripheral demyelination |
Delayed myelination |
Lateral ventricle dilatation |
Hydrocephalus |
Communicating hydrocephalus |
Subependymal nodules |
Ventriculomegaly |
Open operculum |
Abnormal basal ganglia morphology |
T2 hypointense basal ganglia |
Abnormal caudate nucleus morphology |
Abnormal putamen morphology |
Pallidal degeneration |
Abnormal cerebral white matter morphology |
Widened subarachnoid space |
Ataxia |
Poor motor coordination |
Athetosis |
Choreoathetosis |
Chorea |
Tremor |
Delayed speech and language development |
Dysarthria |
Cognitive impairment |
Dementia |
Loss of consciousness |
Dystonia |
Limb dystonia |
Encephalopathy |
Infantile encephalopathy |
Headache |
Developmental regression |
Global developmental delay |
Peripheral neuropathy |
Seizure |
Infantile spasms |
| Disease(s) Associated with GCDH | ||||||||||||||||||||||||||||||||||||||||
| glutaric acidemia I |
| Mouse Phenotypes | neurodegeneration |
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| Availability | Mouse Genotype | |
| Gcdhtm1Dmk/Gcdhtm1Dmk | ||
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 04/30/2024 MGI 6.23 |
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