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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: Nephrosis (D009401)
Parent Node: Pulmonary Valve Stenosis (D011666)
..Starting node ..Pulmonic Stenosis and Congenital Nephrosis (C562895)
Child Nodes:
Sister Nodes:
..Ciuffo Syndrome (C566733)
..Hordnes Engebretsen Knudtson syndrome (C536067)
..Keutel syndrome (C536167)
..LEOPARD Syndrome (D044542) 2
..Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness (C562894)
..Pulmonary Subvalvular Stenosis (D011662)
..Pulmonic Stenosis and Congenital Nephrosis (C562895)
..WATSON SYNDROME (OMIM:193520)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9502
Name:	Pulmonic Stenosis and Congenital Nephrosis
Definition:
Alternative IDs:
ParentIDs:	MESH:D009401\|MESH:D011666
TreeNumbers:	C12.777.419.630/C562895 \|C13.351.968.419.630/C562895 \|C14.280.484.716/C562895 \|C14.280.955.750/C562895
Synonyms:
Slim Mappings:	Cardiovascular disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C562895 MeSH: C562895 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants