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: Death (D003643)
..Starting node ..Parental Death (D063129)
Child Nodes:
........Maternal Death (D063130)
Sister Nodes:
..Asphyxia (D001237)
..Brain Death (D001926)
..Cadaver (D002102) 4
..Death, Sudden (D003645) 7
..Drowning (D004332) 1
..Embryo Loss (D020964)
..Fetal Death (D005313) 4
..Infant Death (D066088) 2
..Parental Death (D063129) 1
..Perinatal Death (D066087)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8641
Name:	Parental Death
Definition:	The death of the father or mother or another person in this role.
Alternative IDs:
ParentIDs:	MESH:D003643
TreeNumbers:	C23.550.260.730
Synonyms:	Death, Parental \|Death, Paternal \|Deaths, Parental \|Deaths, Paternal \|Parental Deaths \|Paternal Death \|Paternal Deaths
Slim Mappings:	Pathology (process)
Reference:	MedGen: D063129 MeSH: D063129 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants