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Holoprosencephaly 1
rareThe 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.
- Identifiers
- MONDO:0009349 OMIM:236100
- Part of
- Holoprosencephaly
- Also known as
- holoprosencephaly 1, isolated cases · holoprosencephaly type 1 · HPE1
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