Search Ontology:
Human Disease

Fraser syndrome 1

Term ID
DOID:0111405
Synonyms
  • FRASRS1
Definition
A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21.21. https://www.ncbi.nlm.nih.gov/pubmed/12766769
References
Ontology
Human Disease   ( DOID:0111405 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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