Visualize Submit Comment
Metadata
ID DOID:0080591
Name Klippel-Feil syndrome 3
Definition A Klippel-Feil syndrome that has_material_basis_in heterozygous mutation in the GDF3 gene on chromosome 12p13.
https://www.ncbi.nlm.nih.gov/pubmed/19864492
Xrefs

MIM:613702

Parent Relationships

is_a Klippel-Feil syndrome

is_a autosomal dominant disease

Add an item to the term tracker