OBO ID: DOID:0111407
Term Name: Fraser syndrome 2 Search Ontology:
Synonyms:
  • FRASRS2
Definition: A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FREM2 gene on chromosome 13q13.3. https://www.ncbi.nlm.nih.gov/pubmed/15838507
References:
Ontology: Human Disease   ( DOID:0111407 )
Relationships
is a type of:
OTHER Fraser syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FREM2 Fraser syndrome 2 617666
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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