Search Ontology:
Human Disease

Pfeiffer syndrome

Term ID
DOID:14705
Synonyms
  • acrocephalosyndactylia type V
Definition
An acrocephalosyndactylia that has_material_basis_in mutations in the FGFR1 and FGFR2 gene which results_in premature fusion located_in skull. (4)
References
Ontology
Human Disease   ( DOID:14705 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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