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Term ID: | 2792 |
Name: | COUSIN SYNDROME |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:C535550|MESH:D006130|MESH:D019465 |
TreeNumbers: | C05.116.099.370/C535550/260660 |C05.660.207/260660 |C16.131.621.207/260660 |C23.550.393/260660 |
Synonyms: | CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORT STATURE |PELVISCAPULAR DYSPLASIA |
Slim Mappings: | Congenital abnormality|Musculoskeletal disease|Pathology (process) |
Reference: |
MedGen: 260660
MeSH: 260660
OMIM: 260660;
Genes: TBX15; | Phenotypes | | Disease Causing ClinVar Variants | |
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