Holoprosencephaly 3

MONDO:0007733

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

Also known as: HLP3, HPE3, SHH holoprosencephaly, Shh holoprosencephaly, holoprosencephaly 3, holoprosencephaly caused by mutation in SHH, holoprosencephaly caused by mutation in Shh, holoprosencephaly type 3

10 clinical trials for this condition and its sub-types.

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