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Holoprosencephaly 4
MONDO:0007734A rare disorder caused by mutations in the TGIF gene mapped to chromosome 18p11.3. It is characterized by semilobar holoprosencephaly, hypotelorism, and ptosis.
Also known as: HPE4, TGIF1 holoprosencephaly, holoprosencephaly 4, holoprosencephaly caused by mutation in TGIF1, holoprosencephaly type 4
10 clinical trials for this condition and its sub-types.
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