Holoprosencephaly 7

MONDO:0012562

Any holoprosencephaly in which the cause of the disease is a mutation in the PTCH1 gene.

Also known as: HPE7, PTCH1 holoprosencephaly, holoprosencephaly 7, holoprosencephaly caused by mutation in PTCH1, holoprosencephaly type 7

0 clinical trials for this condition and its sub-types, 0 tagged with Holoprosencephaly 7 itself.

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