Disease browser and phenotype portal

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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: Metaplasia (D008679)
..Starting node ..Neovascularization, Pathologic (D009389)
Child Nodes:
........Choroidal Neovascularization (D020256)
........Eales disease (C538011)
........Retinal Neovascularization (D015861)
Sister Nodes:
..Neovascularization, Pathologic (D009389) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7864
Name:	Neovascularization, Pathologic
Definition:	A pathologic process consisting of the proliferation of blood vessels in abnormal tissues or in abnormal positions.
Alternative IDs:
ParentIDs:	MESH:D008679
TreeNumbers:	C23.550.589.500
Synonyms:	Angiogenesis, Pathologic \|Angiogenesis, Pathological \|Neovascularization, Pathological \|Pathological Angiogenesis \|Pathological Neovascularization \|Pathologic Angiogenesis \|Pathologic Neovascularization
Slim Mappings:	Pathology (process)
Reference:	MedGen: D009389 MeSH: D009389 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants