Term ID: | 9962 |
Name: | Sanderson Fraser syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D000015|MESH:D005094|MESH:D006228|MESH:D010855 |
TreeNumbers: | C05.390.408/C537232 |C05.500.460.606/C537232 |C05.660.207.540.460.606/C537232 |C05.660.585.988.425/C537232 |C07.320.440.606/C537232 |C07.650.500.460.606/C537232 |C11.675.349/C537232 |C16.131.077/C537232 |C16.131.621.207.540.460.606/C537232 |C16.131.621.585.425/C5 |
Synonyms: | Proptosis, Robin association, clenched hands, and multiple abnormalities |
Slim Mappings: | Congenital abnormality|Eye disease|Mouth disease|Musculoskeletal disease |
Reference: |
MedGen: C537232
MeSH: C537232
OMIM:
Genes: |
Phenotypes | |
Disease Causing ClinVar Variants | |