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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: Abdominal Injuries (D000007)
Parent Node: Hernia, Diaphragmatic (D006548)
..Starting node ..Hernia, Diaphragmatic, Traumatic (D006549)
Child Nodes:
Sister Nodes:
..Diaphragm, Complete Agenesis Of (C564189)
..Diaphragmatic Hernia 1 (C564188)
..Diaphragmatic Hernia 2 (C565629)
..Diaphragmatic Hernia 3 (C565710)
..Fryns syndrome (C538070)
..Hernia, Diaphragmatic, Traumatic (D006549)
..Hernia, Hiatal (D006551) 3
..Hernias, Diaphragmatic, Congenital (D065630) 7
..Jarcho-Levin syndrome (C537565) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5134
Name:	Hernia, Diaphragmatic, Traumatic
Definition:	The type of DIAPHRAGMATIC HERNIA caused by TRAUMA or injury, usually to the ABDOMEN.
Alternative IDs:
ParentIDs:	MESH:D000007\|MESH:D006548
TreeNumbers:	C23.300.707.500.233 \|C26.017.258
Synonyms:	Diaphragmatic Hernias, Traumatic \|Diaphragmatic Hernia, Traumatic \|Hernias, Traumatic Diaphragmatic \|Hernia, Traumatic Diaphragmatic \|Traumatic Diaphragmatic Hernia \|Traumatic Diaphragmatic Hernias
Slim Mappings:	Pathology (anatomical condition)\|Wounds and injuries
Reference:	MedGen: D006549 MeSH: D006549 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants