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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: Hamartoma (D006222)
Parent Node: Heart Defects, Congenital (D006330)
Parent Node: Syndactyly (D013576)
Parent Node: Tongue Neoplasms (D014062)
..Starting node ..Orstavik Lindemann Solberg syndrome (C537137)
Child Nodes:
Sister Nodes:
..Orstavik Lindemann Solberg syndrome (C537137)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8353
Name:	Orstavik Lindemann Solberg syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D006222\|MESH:D006330\|MESH:D013576\|MESH:D014062
TreeNumbers:	C04.445/C537137 \|C04.588.443.591.925/C537137 \|C05.116.099.370.894.819/C537137 \|C05.660.585.800/C537137 \|C05.660.906.819/C537137 \|C07.465.565.925/C537137 \|C07.465.910.874/C537137 \|C14.240.400/C537137 \|C14.280.400/C537137 \|C16.131.240.400/C537137 \|C16.131.621.585.80
Synonyms:	Congenital heart defects, hamartomas of tongue, and polysyndactyly
Slim Mappings:	Cancer\|Cardiovascular disease\|Congenital abnormality\|Mouth disease\|Musculoskeletal disease
Reference:	MedGen: C537137 MeSH: C537137 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants