Disease Browser
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Parent Node: Ataxia (D001259) | Parent Node: Lipidoses (D008064) | Parent Node: Tremor (D014202) | ..Starting node ..Tremor of Intention, Ataxia, and Lipofuscinosis (C566038)
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Sister Nodes: | ..Fragile X Tremor Ataxia Syndrome (C564105)
| ..Geniospasm (C537682)
| ..MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354)
| ..Primary orthostatic tremor (C536418)
| ..Tremor hereditary essential, 2 (C536546)
| ..Tremor of Intention, Ataxia, and Lipofuscinosis (C566038)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 11219 |
Name: | Tremor of Intention, Ataxia, and Lipofuscinosis |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D001259|MESH:D008064|MESH:D014202 |
TreeNumbers: | C10.597.350.090/C566038 |C10.597.350.850/C566038 |C16.320.565.398.641/C566038 |C18.452.584.687/C566038 |C18.452.648.398.641/C566038 |C23.888.592.350.090/C566038 |C23.888.592.350.850/C566038 |
Synonyms: | |
Slim Mappings: | Genetic disease (inborn)|Metabolic disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C566038
MeSH: C566038
OMIM: 190200;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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