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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Genetic Diseases, X-Linked (D040181)
Parent Node: Parkinson Disease (D010300)
..Starting node ..Parkinson Disease 12 (C564486)
Child Nodes:
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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8653
Name:	Parkinson Disease 12
Definition:
Alternative IDs:	OMIM:300557
ParentIDs:	MESH:D010300\|MESH:D040181
TreeNumbers:	C10.228.140.079.862.500/C564486 \|C10.228.662.600.400/C564486 \|C10.574.812/C564486 \|C16.320.322/C564486
Synonyms:	PARK12 \|Parkinson Disease, X-Linked
Slim Mappings:	Genetic disease (inborn)\|Nervous system disease
Reference:	MedGen: C564486 MeSH: C564486 OMIM: 300557; Genes: PARK12;
Phenotypes
Disease Causing ClinVar Variants