Holoprosencephaly 11
MONDO:0013642Any holoprosencephaly in which the cause of the disease is a mutation in the CDON gene.
Also known as: CDON holoprosencephaly, HPE11, holoprosencephaly 11, holoprosencephaly caused by mutation in CDON, holoprosencephaly type 11
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)