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: Congenital Abnormalities (D000013)
Parent Node: Radiation Injuries (D011832)
..Starting node ..Abnormalities, Radiation-Induced (D000016)
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:	85
Name:	Abnormalities, Radiation-Induced
Definition:	Congenital changes in the morphology of organs produced by exposure to ionizing or non-ionizing radiation.
Alternative IDs:
ParentIDs:	MESH:D000013\|MESH:D011832
TreeNumbers:	C16.131.080 \|C26.733.031
Synonyms:	Abnormalities, Radiation Induced \|Abnormality, Radiation-Induced \|Radiation Induced Abnormalities \|Radiation-Induced Abnormalities \|Radiation-Induced Abnormality
Slim Mappings:	Congenital abnormality\|Wounds and injuries
Reference:	MedGen: D000016 MeSH: D000016 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants