Disease Browser
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Parent Node: Mitochondrial Diseases (D028361) | Parent Node: Parkinson Disease (D010300) | ..Starting node ..Parkinson Disease, Mitochondrial (C564015)
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Sister Nodes: | ..AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1 (OMIM:105500)
| ..Paralysis Agitans, Juvenile, Of Hunt (C562469)
| ..PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (OMIM:168601)
| ..Parkinson Disease 10 (C564653)
| ..Parkinson Disease 11 (C564345)
| ..PARKINSON DISEASE 11, AUTOSOMAL DOMINANT (OMIM:607688)
| ..Parkinson Disease 12 (C564486)
| ..Parkinson Disease 13 (C565204)
| ..PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO (OMIM:610297)
| ..PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE (OMIM:612953)
| ..Parkinson Disease 16 (C567726)
| ..Parkinson disease 3 (C537176)
| ..Parkinson Disease 3, Autosomal Dominant Lewy Body (C566552)
| ..Parkinson Disease 4, Autosomal Dominant Lewy Body (C565324)
| ..PARKINSON DISEASE 5, AUTOSOMAL DOMINANT (OMIM:613643)
| ..Parkinson Disease 6, Autosomal Recessive Early-Onset (C565276)
| ..Parkinson Disease 7, Autosomal Recessive Early-Onset (C565238)
| ..PARKINSON DISEASE 8, AUTOSOMAL DOMINANT (OMIM:607060)
| ..Parkinson Disease, Familial, Type 1 (C566823)
| ..PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
| ..Parkinson Disease, Mitochondrial (C564015)
| ..Parkinsonism, early onset with mental retardation (C537179)
| ..Parkinsonism-Dystonia, Infantile (C567730)
| ..Progressive supranuclear palsy atypical (C537240)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 8671 |
Name: | Parkinson Disease, Mitochondrial |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D010300|MESH:D028361 |
TreeNumbers: | C10.228.140.079.862.500/C564015 |C10.228.662.600.400/C564015 |C10.574.812/C564015 |C18.452.660/C564015 |
Synonyms: | |
Slim Mappings: | Metabolic disease|Nervous system disease |
Reference: |
MedGen: C564015
MeSH: C564015
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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