Curators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.
CL: Cell Ontology
primary motor cortex pyramidal cell
EFO: Experimental Factor Ontology
autism spectrum disorder
brain abnormalities, neurodegeneration, and dysosteosclerosis ceroid lipofuscinosis, neuronal, 6A Cognitive regression congenital structural myopathy d-bifunctional protein deficiency Dehydratase deficiency Delayed gross motor development developmental and epileptic encephalopathy, 39 developmental delay with autism spectrum disorder and gait instability Developmental regression Developmental stagnation Developmental stagnation at onset of seizures dihydropyrimidine dehydrogenase deficiency Global developmental delay global developmental delay, progressive ataxia, and elevated glutamine hereditary sensory and autonomic neuropathy type 7
impaired psychomotor skills
intellectual disability with language impairment intellectual disability-severe speech delay-mild dysmorphism syndrome
learning disability
mathematical ability
metachromatic leukodystrophy, juvenile form mitochondrial complex IV deficiency, nuclear type 19 Motor delay
motor development measurement
neurobehavioral manifestations
Neurodevelopmental delay neurodevelopmental disorder with macrocephaly and with or without seizures neurodevelopmental disorder with poor language and loss of hand skills
neurodevelopmental measurement
neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 9
oral motor function measurement
pervasive developmental disorder
Poor fine motor coordination
posterior cortical atrophy
pterin-4 alpha-carbinolamine dehydratase 1 deficiency Siddiqi syndrome ski-like protein ski-like protein (human) SKIL (human) Snijders Blok-Fisher syndrome Specific learning disability SSR4-congenital disorder of glycosylation