Term ID: | 9887 |
Name: | Robin sequence and oligodactyly |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D010855 |
TreeNumbers: | C05.500.460.606/C535688 |C05.660.207.540.460.606/C535688 |C07.320.440.606/C535688 |C07.650.500.460.606/C535688 |C16.131.621.207.540.460.606/C535688 |C16.131.850.500.460.606/C535688 |
Synonyms: | Pierre Robin syndrome and oligodactyly |
Slim Mappings: | Congenital abnormality|Mouth disease|Musculoskeletal disease |
Reference: |
MedGen: C535688
MeSH: C535688
OMIM:
Genes: |
Phenotypes | |
Disease Causing ClinVar Variants | |