Search Ontology:
Human Disease

Fraser syndrome 2

Term ID
DOID:0111407
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 Pages
Genes Involved
Zebrafish Models