Disease #02064 (schizencephaly (schizencephaly), OMIM:269160)

Official abbreviation schizencephaly
Name schizencephaly
OMIM ID 269160
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 3 genes EMX2, SHH, SIX3
Associated tissues -
Disease features -
Remarks -