Holoprosencephaly 3
MONDO:0007733Any holoprosencephaly in which the cause of the disease is a mutation in the SHH gene.
Also known as: HLP3, HPE3, SHH holoprosencephaly, Shh holoprosencephaly, holoprosencephaly 3, holoprosencephaly caused by mutation in SHH, holoprosencephaly caused by mutation in Shh, holoprosencephaly type 3
10 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
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)