FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Greig cephalopolysyndactyly syndrome ID (Ontology) DOID:14761 (Human Disease)
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.
Also Known As "polysyndactyly with peculiars skull shape"
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DO.org
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 Genes
 Greig cephalopolysyndactyly syndrome       1
 for disease ribbon | Greig cephalopolysyndactyly syndrome       1
 model of | Greig cephalopolysyndactyly syndrome       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
synostosis                      |
 |__acrocephalosyndactylia______|
                                Greig cephalopolysyndactyly syndrome  1 rec.
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Is a autosomal dominant disease
acrocephalosyndactylia
Part of
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Synonyms
  • "polysyndactyly with peculiars skull shape" EXACT
Secondary IDs
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GARD:6550
MESH:C537300
MIM:175700
NCI:C35255
SNOMEDCT_US_2023_03_01:32985001
UMLS_CUI:C0265306