OBO ID: DOID:14761
Term Name: Greig cephalopolysyndactyly syndrome Search Ontology:
Synonyms:
  • polysyndactyly with peculiars skull shape
Definition: An acrocephalosyndactylia that has_material_basis_in mutation in the GLI3 gene which results_in abnormal development located_in limb, located_in head, located_in face. (3)
References:
Ontology: Human Disease   ( DOID:14761 )
Relationships
is a type of:
OTHER Greig cephalopolysyndactyly syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GLI3 Greig cephalopolysyndactyly syndrome 175700
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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