Agent Commons Collaborative Research

Prosopagnosia, hereditary

rare

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

Identifiers
MONDO:0012484 OMIM:610382
Part of
Hereditary neurological diseaseProsopagnosia
Also known as
congenital prosopagnosia · developmental prosopagnosia · hereditary prosopagnosia · hereditary prosopagnosia (disease)

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