Holoprosencephaly 11

MONDO:0013642

Any holoprosencephaly in which the cause of the disease is a mutation in the CDON gene.

Also known as: CDON holoprosencephaly, HPE11, holoprosencephaly 11, holoprosencephaly caused by mutation in CDON, holoprosencephaly type 11

0 clinical trials for this condition and its sub-types, 0 tagged with Holoprosencephaly 11 itself.

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