Cortical Blindness

Alias:

Blindness, Cortical

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cortical Blindness, also known as blindness, cortical, is related to neurodevelopmental disorder with hypotonia, microcephaly, and seizures and visual agnosia, and has symptoms including amaurosis fugax An important gene associated with Cortical Blindness is DOCK7 (Dedicator Of Cytokinesis 7), and among its related pathways/superpathways are Peroxisomal lipid metabolism and Complex I biogenesis. Affiliated tissues include cortex and eye, and related phenotypes are Reduced mammosphere formation and nervous system

Related ID：

MALACARDS：CRT012

MESH：D019575