Terminology Service for NFDI4Health
holoprosencephaly 2
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http://purl.obolibrary.org/obo/DOID_0110872
A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21. [ http://purl.obolibrary.org/obo/ECO_0007645 ]