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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: Diabetic Angiopathies (D003925)
Parent Node: Diabetic Nephropathies (D003928)
..Starting node ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (OMIM:612628)
Child Nodes:
Sister Nodes:
..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1 (OMIM:603933)
..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (OMIM:612628)
..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (OMIM:612633)
..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (OMIM:612634)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7264
Name:	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4
Definition:
Alternative IDs:
ParentIDs:	MESH:D003925\|MESH:D003928
TreeNumbers:	C12.777.419.192/612628 \|C13.351.968.419.192/612628 \|C14.907.320/612628 \|C19.246.099.500/612628 \|C19.246.099.875/612628
Synonyms:	MVCD4 \|NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO
Slim Mappings:	Cardiovascular disease\|Endocrine system disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: 612628 MeSH: 612628 OMIM: 612628; Genes: IL1RN;
Phenotypes
Disease Causing ClinVar Variants