Holoprosencephaly 9

MONDO:0012563

Any holoprosencephaly in which the cause of the disease is a mutation in the GLI2 gene.

Also known as: GLI2 holoprosencephaly, HPE9, holoprosencephaly 9, holoprosencephaly caused by mutation in GLI2, holoprosencephaly type 9, holoprosencephaly with microphthalmia and first branchial arch anomalies, pituitary anomalies with holoprosencephaly-like features, holoprosencephaly with microphthalmia and first branchial Arch anomalies

0 clinical trials for this condition and its sub-types, 0 tagged with Holoprosencephaly 9 itself.

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↑ Alobar holoprosencephaly (0) ↑ Lobar holoprosencephaly (0) ↑ Microform holoprosencephaly (0)

Including sub-types (0) Tagged with Holoprosencephaly 9 (0)

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