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familial schizencephaly

Disease Summary
Associated Targets (4)
Tbio

3

Tchem

1


Explore Associated Targets
Mondo Description An instance of schizencephaly that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0018829:  familial schizencephaly
MESH:C538514: 
Orphanet:481986: 
UMLS:C2931870: 
UMLS:CN776926: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found