Holoprosencephaly 4

MONDO:0007734

A 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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