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: Leukemia (D007938)
Parent Node: Neoplasms, Radiation-Induced (D009381)
Parent Node: Radiation Injuries (D011832)
..Starting node ..Leukemia, Radiation-Induced (D007953)
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:	6367
Name:	Leukemia, Radiation-Induced
Definition:	Leukemia produced by exposure to IONIZING RADIATION or NON-IONIZING RADIATION.
Alternative IDs:
ParentIDs:	MESH:D007938\|MESH:D009381\|MESH:D011832
TreeNumbers:	C04.557.337.650 \|C04.682.512 \|C26.733.345
Synonyms:	Leukemia, Radiation Induced \|Leukemias, Radiation-Induced \|Radiation Induced Leukemia \|Radiation-Induced Leukemia \|Radiation-Induced Leukemias
Slim Mappings:	Cancer\|Wounds and injuries
Reference:	MedGen: D007953 MeSH: D007953 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants