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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: Neoplasms (D009369)
..Starting node ..Neoplasms, Second Primary (D016609)
Child Nodes:
Sister Nodes:
..abc disease (C579754)
..Chromosomal Instability with Tissue-Specific Radiosensitivity (C565848)
..Cysts (D003560) 78
..Hamartoma (D006222) 26
..Neoplasms by Histologic Type (D009370) 696
..Neoplasms by Site (D009371) 492
..Neoplasms, Experimental (D009374) 37
..Neoplasms, Hormone-Dependent (D009376)
..Neoplasms, Multiple Primary (D009378) 24
..Neoplasms, Post-Traumatic (D017169)
..Neoplasms, Radiation-Induced (D009381) 3
..Neoplasms, Second Primary (D016609)
..Neoplastic Processes (D009385) 18
..Neoplastic Syndromes, Hereditary (D009386) 111
..Paraneoplastic Syndromes (D010257) 16
..Precancerous Conditions (D011230) 29
..Pregnancy Complications, Neoplastic (D011252) 7
..Tumor Virus Infections (D014412) 20
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7857
Name:	Neoplasms, Second Primary
Definition:	Abnormal growths of tissue that follow a previous neoplasm but are not metastases of the latter. The second neoplasm may have the same or different histological type and can occur in the same or different organs as the previous neoplasm but in all cases arises from an independent oncogenic event. The development of the second neoplasm may or may not be related to the treatment for the previous neoplasm since genetic risk or predisposing factors may actually be the cause.
Alternative IDs:
ParentIDs:	MESH:D009369
TreeNumbers:	C04.692
Synonyms:	Cancer, Second \|Cancer, Second Primary \|Cancers, Second \|Cancers, Second Primary \|Cancers, Therapy-Associated \|Cancers, Therapy-Related \|Cancers, Treatment-Associated \|Cancers, Treatment-Related \|Cancer, Therapy-Associated \|Cancer, Therapy-Related \|Cancer, Treatme
Slim Mappings:	Cancer
Reference:	MedGen: D016609 MeSH: D016609 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants