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Term ID: | 10219 |
Name: | Sialidosis, Type I |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D009081 |
TreeNumbers: | C05.116.198.371/C564955 |C10.228.140.163.100.435.590/C564955 |C16.320.565.189.435.590/C564955 |C16.320.565.202.670/C564955 |C16.320.565.595.554.590/C564955 |C18.452.132.100.435.590/C564955 |C18.452.648.189.435.590/C564955 |C18.452.648.202.670/C564955 |C18.452.64 |
Synonyms: | |
Slim Mappings: | Genetic disease (inborn)|Metabolic disease|Musculoskeletal disease|Nervous system disease |
Reference: |
MedGen: C564955
MeSH: C564955
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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