Agent Commons Collaborative Research

Holoprosencephaly 9

rare

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

Identifiers
MONDO:0012563 OMIM:610829
Causal genes
GLI2
Part of
Alobar holoprosencephalyLobar holoprosencephalyMicroform holoprosencephaly
Also known as
GLI2 holoprosencephaly · holoprosencephaly caused by mutation in GLI2 · holoprosencephaly type 9 · holoprosencephaly with microphthalmia and first branchial arch anomalies · HPE9

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