Disease Browser
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Parent Node: Supranuclear Palsy, Progressive (D013494) | ..Starting node ..Supranuclear Palsy, Progressive, 3 (C567050)
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Sister Nodes: | ..Familial progressive supranuclear palsy (C538572)
| ..Progressive supranuclear palsy atypical (C537240)
| ..Supranuclear Palsy, Progressive, 2 (C563717)
| ..Supranuclear Palsy, Progressive, 3 (C567050)
| ..Tauopathy and Respiratory Failure (C563580)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
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Term ID: | 11823 |
Name: | Supranuclear Palsy, Progressive, 3 |
Definition: | |
Alternative IDs: | OMIM:610898 |
ParentIDs: | MESH:D013494 |
TreeNumbers: | C10.228.140.079.882/C567050 |C10.228.662.700/C567050 |C10.292.562.750.500/C567050 |C10.574.945.500/C567050 |C10.597.622.447.690/C567050 |C11.590.472.500/C567050 |C23.888.592.636.447.690/C567050 |
Synonyms: | PSNP3 |
Slim Mappings: | Eye disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C567050
MeSH: C567050
OMIM: 610898; MSeqDR : Genes: ERCC2; | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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