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Term ID: | 3367 |
Name: | Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 |
Definition: | |
Alternative IDs: | OMIM:601362 |
ParentIDs: | MESH:D004062 |
TreeNumbers: | C05.660.207.103.500/C563337 |C14.240.400.021.500/C563337 |C14.280.400.044.500/C563337 |C15.604.451.249.500/C563337 |C16.131.077.019.500/C563337 |C16.131.240.400.021.500/C563337 |C16.131.260.019.500/C563337 |C16.131.482.249.500/C563337 |C16.131.621.207.103.500/C5 |
Synonyms: | DGS2 |
Slim Mappings: | Cardiovascular disease|Congenital abnormality|Endocrine system disease|Genetic disease (inborn)|Lymphatic disease|Musculoskeletal disease |
Reference: |
MedGen: C563337
MeSH: C563337
OMIM: 601362;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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