OBO ID: DOID:0080591
Term Name: Klippel-Feil syndrome 3 Search Ontology:
Synonyms:
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
References:
Ontology: Human Disease   ( DOID:0080591 )
Relationships
is a type of:
OTHER Klippel-Feil syndrome 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GDF3 Klippel-Feil syndrome 3, autosomal dominant 613702
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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