Term ID: | 1874 |
Name: | Catel Manzke syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D006228|MESH:D010855 |
TreeNumbers: | C05.390.408/C535347 |C05.500.460.606/C535347 |C05.660.207.540.460.606/C535347 |C05.660.585.988.425/C535347 |C07.320.440.606/C535347 |C07.650.500.460.606/C535347 |C16.131.621.207.540.460.606/C535347 |C16.131.621.585.425/C535347 |C16.131.850.500.460.606/C535347 |
Synonyms: | Catel-Manzke Syndrome |Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome |Index Finger Anomaly With Pierre Robin Syndrome |Palatodigital syndrome, Catel-Manzke type |Pierre Robin syndrome with hyperphalangy and clinodactyly |
Slim Mappings: | Congenital abnormality|Mouth disease|Musculoskeletal disease |
Reference: |
MedGen: C535347
MeSH: C535347
OMIM:
Genes: |
Phenotypes | |
Disease Causing ClinVar Variants | |