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Holoprosencephaly
MONDO:0016296Holoprosencephaly (HPE) is a complex brain malformation resulting from incomplete cleavage of the prosencephalon, occurring between the 18th and 28th day of gestation, and affecting both the forebrain and face, which results in neurological manifestations and facial anomalies of variable severity.
Also known as: HPE, holoprosencephaly sequence
10 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Alobar holoprosencephaly
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Chromosome 1q41-q42 deletion syndrome
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Holoprosencephaly 1
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Holoprosencephaly 10
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Holoprosencephaly 11
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Holoprosencephaly 12 with or without pancreatic agenesis
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Holoprosencephaly 13, X-linked
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Holoprosencephaly 14
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Holoprosencephaly 2
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Holoprosencephaly 3
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Holoprosencephaly 4
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Holoprosencephaly 5
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Holoprosencephaly 6
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Holoprosencephaly 7
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Holoprosencephaly 8
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Holoprosencephaly 9
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Lobar holoprosencephaly
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Microform holoprosencephaly
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Semilobar holoprosencephaly
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Solitary median maxillary central incisor syndrome
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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)