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holoprosencephaly 1

Disease Summary
Associated Targets ()

Mondo Description The 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.
Mondo Term and Equivalent IDs
MONDO:0009349:  holoprosencephaly 1
NCIT:C75476: 
Orphanet:268936: