Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Hernia, Abdominal (D046449)
..Starting node ..Hernia, Inguinal (D006552)
Child Nodes:
........Arthrogryposis multiplex with deafness, inguinal hernias, and early death (C535381)
........Hernia, Double Inguinal (C563164)
........Lambert syndrome (C538396)
........Microspherophakia with hernia (C537468)
Sister Nodes:
..Diverticulosis of Bowel, Hernia, and Retinal Detachment (C565619)
..Gastroschisis (D020139) 1
..Hernia, Femoral (D006550)
..Hernia, Inguinal (D006552) 4
..Hernia, Ventral (D006555) 7
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5138
Name:	Hernia, Inguinal
Definition:	An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur through the internal inguinal ring. Direct inguinal hernias occur through defects in the ABDOMINAL WALL (transversalis fascia) in Hesselbach's triangle. The former type is commonly seen in children and young adults; the latter in adults.
Alternative IDs:
ParentIDs:	MESH:D046449
TreeNumbers:	C23.300.707.374.875
Synonyms:	Direct Inguinal Hernia \|Direct Inguinal Hernias \|Hernia, Direct Inguinal \|Hernia, Indirect Inguinal \|Hernias, Direct Inguinal \|Hernias, Indirect Inguinal \|Hernias, Inguinal \|Indirect Inguinal Hernia \|Indirect Inguinal Hernias \|Inguinal Hernia \|Inguinal Hernia, Dir
Slim Mappings:	Pathology (anatomical condition)
Reference:	MedGen: D006552 MeSH: D006552 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants