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familial porencephaly

Disease Summary
Associated Targets (2)
Tbio

2


Mondo Description An instance of porencephaly that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0020496:  familial porencephaly
GARD:0002258: 
OMIMPS:175780: 
Orphanet:99810: