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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: Ectromelia (D004480)
Parent Node: Kidney Diseases (D007674)
Parent Node: Urethral Obstruction (D014524)
..Starting node ..Selig Benacerraf Greene syndrome (C535840)
Child Nodes:
Sister Nodes:
..Cervical ribs sprengel anomaly anal atresia urethral obstruction (C538072)
..Kashani Strom Utley syndrome (C537010)
..Selig Benacerraf Greene syndrome (C535840)
..Urethral obstruction sequence (C536477)
..Urethral Stricture (D014525)
..Urinary Bladder Neck Obstruction (D001748)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10115
Name:	Selig Benacerraf Greene syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D004480\|MESH:D007674\|MESH:D014524
TreeNumbers:	C05.660.585.350/C535840 \|C12.777.419/C535840 \|C12.777.767.700/C535840 \|C13.351.968.419/C535840 \|C13.351.968.767.700/C535840 \|C16.131.621.585.350/C535840
Synonyms:	Renal dysplasia, megalocystis, and sirenomelia
Slim Mappings:	Congenital abnormality\|Musculoskeletal disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C535840 MeSH: C535840 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants