An instance of prosopagnosia (disease) that is caused by an inherited modification of the individual's genome.
Comprehensive, easy-to-understand information about this condition
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leukoencephalopathy, megalencephalic
MONDO:0000137
epilepsy, familial adult myoclonic
MONDO:0000160
encephalopathy, acute, infection-induced
MONDO:0000166
GLUT1 deficiency syndrome
MONDO:0000188
paraganglioma
MONDO:0000448
familial hemiplegic migraine
MONDO:0000700