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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: Diabetes Mellitus (D003920)
Parent Node: Heart Diseases (D006331)
Parent Node: Intellectual Disability (D008607)
Parent Node: Nephritis (D009393)
..Starting node ..Yorifuji Okuno syndrome (C536714)
Child Nodes:
Sister Nodes:
..Dyschondrosteosis and Nephritis (C565080)
..Glomerulonephritis (D005921) 21
..Hypertensive Nephropathy (C563161)
..Nephritis, Hereditary (D009394) 11
..Nephritis, Interstitial (D009395) 8
..Pyelitis (D011702) 3
..SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 1 (OMIM:607965)
..SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2 (OMIM:607966)
..SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3 (OMIM:607967)
..Yorifuji Okuno syndrome (C536714)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11858
Name:	Yorifuji Okuno syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D003920\|MESH:D006331\|MESH:D008607\|MESH:D009393
TreeNumbers:	C10.597.606.643/C536714 \|C12.777.419.570/C536714 \|C13.351.968.419.570/C536714 \|C14.280/C536714 \|C18.452.394.750/C536714 \|C19.246/C536714 \|C23.888.592.604.646/C536714 \|F03.550.600/C536714
Synonyms:	Pancreatic hypoplasia diabetes heart disease
Slim Mappings:	Cardiovascular disease\|Endocrine system disease\|Mental disorder\|Metabolic disease\|Nervous system disease\|Signs and symptoms\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C536714 MeSH: C536714 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants