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Metadata
ID DOID:0110880
Name holoprosencephaly 4
Definition A holoprosencephaly that has_material_basis_in heterozygous mutation in the TGIF gene on chromosome 18p11.
https://www.ncbi.nlm.nih.gov/pubmed/10835638, https://www.ncbi.nlm.nih.gov/pubmed/16323008
Xrefs

MESH:C564180

OMIM:142946

Synonyms

HPE4 [EXACT]

Parent Relationships

is_a holoprosencephaly

is_a autosomal dominant disease

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