Visualize Submit Comment
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/16323008, https://www.ncbi.nlm.nih.gov/pubmed/10835638
Xrefs

MESH:C564180

MIM:142946

Synonyms

HPE4 [EXACT]

Parent Relationships

is_a autosomal dominant disease

is_a holoprosencephaly

Subclass Logical Relationships

has material basis in some autosomal dominant inheritance

Add an item to the term tracker