Disease Info Card

Learning Disorders

Information about Learning Disorders: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Learning Disorders

Most recent studies have shown that Learning Disorders shares some biological mechanisms with affective-symptoms, anxiety-disorders, attention-deficit-hyperactivity-disorder, autistic-disorder, brain-damage-chronic, child-behavior-disorders, cognition-disorders, depressive-disorder, developmental-disabilities, dyslexia, epilepsy, impairment-(finding), language-disorders, learning-disabilities, malnutrition, memory-disorders, memory-impairment, mental-disorders.

Among the many pathways, these few ones have gauged particular interests from scientists studying Learning Disorders, and have been seen in publications frequently: Aging, Associative Learning, Brain Development, Cell Adhesion, Cell Death, Cognition, Habituation, Localization, Locomotion, Long-term Memory, Neurogenesis, Pathogenesis, Reflex, Short-term Memory, Social Behavior, Swimming, Synaptic Transmission, Translation, Visual Learning, Visual Perception

Quite a number of genes have been found to play important roles in Learning Disorders, such as ACHE, APP, ARNTL, ARSA, BDNF, CA1, CA3, CHAT, ERMAP, FMN1, FMR1, FOXC2, NF1, NHS, PEX7, PHYH, SLC17A5. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Learning Disorders Related Genes

click to see detail information for each gene

ACHE APP ARNTL
ARSA BDNF CA1
CA3 CHAT ERMAP
FMN1 FMR1 FOXC2
NF1 NHS PEX7
PHYH SLC17A5