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

• OMIM:617667

Ontology

Human Disease   ( DOID:0111406 )