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

• OMIM:617666

Ontology

Human Disease   ( DOID:0111407 )