Holoprosencephaly 5
MONDO:0012322Holoprosencephaly associated with mutations in the ZIC2 gene.
Also known as: HPE5, ZIC2 holoprosencephaly, holoprosencephaly 5, holoprosencephaly caused by mutation in ZIC2, holoprosencephaly type 5
10 clinical trials for this condition and its sub-types.
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Disease
(618)
Nervous system disorder
(217)
Hereditary disease
(172)
Endocrine system disorder
(61)
Syndromic disease
(24)
Hereditary endocrine growth disease
(23)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Hereditary neurological disease
(5)
Disease of genetic or genomic mechanism
(2)