Holoprosencephaly 1
MONDO:0009349The most severe form of holoprosencephaly in which there is a complete absence of midline forebrain division resulting in the presence of fused hemispheres and a single ventricle (alobar holoprosencephaly). It is mapped to chromosome 21q22.
Also known as: Hpe, familial, cyclopia, HPE1, holoprosencephaly 1, holoprosencephaly 1, isolated cases, holoprosencephaly type 1, Demyer sequence, arhinencephaly
10 clinical trials for this condition and its sub-types.
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Disease
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Developmental defect during embryogenesis
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