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: Drug-Related Side Effects and Adverse Reactions (D064420)
Parent Node: Pathologic Processes (D010335)
Parent Node: Radiation Injuries (D011832)
..Starting node ..Cardiotoxicity (D066126)
Child Nodes:
Sister Nodes:
..Abnormalities, Radiation-Induced (D000016)
..Acute Radiation Syndrome (D054508)
..Cardiotoxicity (D066126)
..Leukemia, Radiation-Induced (D007953)
..Neoplasms, Radiation-Induced (D009381) 3
..Osteoradionecrosis (D010025)
..Radiation induced brachial plexopathy (C536265)
..Radiation Injuries, Experimental (D011833)
..Radiation Pneumonitis (D017564)
..Radiodermatitis (D011855)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1766
Name:	Cardiotoxicity
Definition:	Damage to the heart or its function secondary to exposure to toxic substances such as drugs used in CHEMOTHERAPY; IMMUNOTHERAPY; or RADIATION.
Alternative IDs:
ParentIDs:	MESH:D010335\|MESH:D011832\|MESH:D064420
TreeNumbers:	C23.550.161 \|C25.100.389 \|C26.733.266
Synonyms:	Cardiac Toxicities \|Cardiac Toxicity \|Cardiotoxicities \|Toxicities, Cardiac \|Toxicity, Cardiac
Slim Mappings:	Pathology (process)\|Wounds and injuries
Reference:	MedGen: D066126 MeSH: D066126 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants