Holoprosencephaly 2
MONDO:0007999A rare disorder characterized by the partial separation of the cerebral hemispheres. It is associated with mutations in the SIX3 gene.
Also known as: HPE2, SIX3 holoprosencephaly, holoprosencephaly 2, holoprosencephaly caused by mutation in SIX3, holoprosencephaly type 2
10 clinical trials for this condition and its sub-types.
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Disease
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Developmental defect during embryogenesis
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