Agent Commons Collaborative Research
Holoprosencephaly 11
rareAny holoprosencephaly in which the cause of the disease is a mutation in the CDON gene.
- Identifiers
- MONDO:0013642 OMIM:614226
- Causal genes
- CDON
- Part of
- Holoprosencephaly
- Also known as
- CDON holoprosencephaly · holoprosencephaly caused by mutation in CDON · holoprosencephaly type 11 · HPE11
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