Intermittent Squint

Alias:

Intermittent Heterotropia

Intermittent Tropia

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Intermittent Squint, also known as intermittent heterotropia, is related to neuromuscular junction disease and congenital myasthenic syndrome. An important gene associated with Intermittent Squint is VAMP1 (Vesicle Associated Membrane Protein 1), and among its related pathways/superpathways are Uptake and actions of bacterial toxins and Nicotine Pathway (Dopaminergic Neuron), Pharmacodynamics. Affiliated tissues include eye, and related phenotypes are Increased shRNA abundance (Z-score > 2) and mortality/aging

Related ID：

MALACARDS：INT008