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Human Disease
Greig cephalopolysyndactyly syndrome
- Term ID
- DOID:14761
- Synonyms
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- 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. (2)
- References
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- GARD:6550
- MESH:C537300
- MIM:175700
- NCI:C35255
- SNOMEDCT_US_2023_03_01:32985001
- UMLS_CUI:C0265306
- Ontology
- Human Disease ( DOID:14761 )
- is a type of
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Genes Involved
Zebrafish Models