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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: Arterial Occlusive Diseases (D001157)
Parent Node: Peripheral Arterial Disease (D058729)
..Starting node ..Peripheral Arterial Occlusive Disease 1 (C564658)
Child Nodes:
Sister Nodes:
..Deafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease (C565120)
..Peripheral Arterial Occlusive Disease 1 (C564658)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8814
Name:	Peripheral Arterial Occlusive Disease 1
Definition:
Alternative IDs:	OMIM:606787
ParentIDs:	MESH:D001157\|MESH:D058729
TreeNumbers:	C14.907.137.126.307.500/C564658 \|C14.907.137/C564658 \|C14.907.617.671/C564658
Synonyms:	PAOD1
Slim Mappings:	Cardiovascular disease
Reference:	MedGen: C564658 MeSH: C564658 OMIM: 606787; Genes:
Phenotypes
Disease Causing ClinVar Variants