Search Ontology:
Human Disease

Fraser syndrome 3

Term ID
DOID:0111406
Synonyms
  • FRASRS3
Definition
A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the GRIP1 gene on chromosome 12q14.3. https://www.ncbi.nlm.nih.gov/pubmed/22510445
References
Ontology
Human Disease   ( DOID:0111406 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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