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Holoprosencephaly 7
MONDO:0012562Any 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
10 clinical trials for this condition and its sub-types.
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