Holoprosencephaly 9
MONDO:0012563Any 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.
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Disease
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Nervous system disorder
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Hereditary disease
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Endocrine system disorder
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Syndromic disease
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Hereditary endocrine growth disease
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Human disease
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Developmental defect during embryogenesis
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Hereditary neurological disease
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Disease of genetic or genomic mechanism
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