OBO ID: DOID:0111406
Term Name: Fraser syndrome 3 Search Ontology:
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 Fraser syndrome 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GRIP1 Fraser syndrome 3 617667
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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