Hearing Loss Disease Portal
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Term ID: | 8338 |
Name: | Orofaciodigital Syndrome 13 |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D009958 |
TreeNumbers: | C05.116.099.370.652/C548035 |C05.660.207.700/C548035 |C16.131.077.677/C548035 |C16.131.260.830.670/C548035 |C16.131.621.207.700/C548035 |C16.320.180.830.670/C548035 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Genetic disease (inborn)|Musculoskeletal disease |
Reference: |
MedGen: C548035
MeSH: C548035
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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