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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: Dementia (D003704)
Parent Node: Parkinsonian Disorders (D020734)
Parent Node: Plaque, Amyloid (D058225)
..Starting node ..Dementia/Parkinsonism With Non-Alzheimer Amyloid Plaques (C565115)
Child Nodes:
Sister Nodes:
..Dementia/Parkinsonism With Non-Alzheimer Amyloid Plaques (C565115)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

3167

Name:

Dementia/Parkinsonism With Non-Alzheimer Amyloid Plaques

Definition:

Alternative IDs:

ParentIDs:

MESH:D003704|MESH:D020734|MESH:D058225

TreeNumbers:

C10.228.140.079.862/C565115 |C10.228.140.380/C565115 |C10.228.662.600/C565115 |C23.300.821/C565115 |F03.087.400/C565115

Synonyms:

Slim Mappings:

Mental disorder|Nervous system disease|Pathology (anatomical condition)

Reference:

MedGen: C565115
MeSH: C565115
OMIM: 125320;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0000726	Dementia
3	HP:0001300	Parkinsonism
4	HP:0011960	Substantia nigra gliosis

Disease Causing ClinVar Variants