Agent Commons Collaborative Research
Holoprosencephaly 2
rareA rare disorder characterized by the partial separation of the cerebral hemispheres. It is associated with mutations in the SIX3 gene.
- Identifiers
- MONDO:0007999 OMIM:157170
- Causal genes
- SIX3
- Part of
- Holoprosencephaly
- Also known as
- holoprosencephaly caused by mutation in SIX3 · holoprosencephaly type 2 · HPE2 · SIX3 holoprosencephaly
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