Prosopagnosia, hereditary

MONDO:0012484

An instance of prosopagnosia (disease) that is caused by an inherited modification of the individual's genome.

Also known as: hereditary prosopagnosia (disease), prosopagnosia, hereditary, congenital prosopagnosia, developmental prosopagnosia, face blindness, hereditary prosopagnosia, prosopagnosia, congenital, prosopagnosia, developmental

0 clinical trials for this condition and its sub-types, 0 tagged with Prosopagnosia, hereditary itself.

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↑ Hereditary neurological disease (5772) ↑ Prosopagnosia (0)

Including sub-types (0) Tagged with Prosopagnosia, hereditary (0)

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