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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: Hernia (D006547)
..Starting node ..Hernia, Abdominal (D046449)
Child Nodes:
........Diverticulosis of Bowel, Hernia, and Retinal Detachment (C565619)
........Gastroschisis (D020139) 1
........Hernia, Femoral (D006550)
........Hernia, Inguinal (D006552) 4
........Hernia, Ventral (D006555) 7
Sister Nodes:
..Acromegaloid features, overgrowth, cleft palate, and hernia (C535656)
..Encephalocele (D004677) 24
..Hernia, Abdominal (D046449) 17
..Hernia, Diaphragmatic (D006548) 20
..Hernia, Obturator (D006553)
..Intervertebral Disc Displacement (D007405) 2
..Megarbane syndrome (C536145)
..Meningocele (D008588) 5
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5131
Name:	Hernia, Abdominal
Definition:	A protrusion of abdominal structures through the retaining ABDOMINAL WALL. It involves two parts: an opening in the abdominal wall, and a hernia sac consisting of PERITONEUM and abdominal contents. Abdominal hernias include groin hernia (HERNIA, FEMORAL; HERNIA, INGUINAL) and VENTRAL HERNIA.
Alternative IDs:
ParentIDs:	MESH:D006547
TreeNumbers:	C23.300.707.374
Synonyms:	Abdominal Hernia \|Abdominal Hernias \|Hernias, Abdominal
Slim Mappings:	Pathology (anatomical condition)
Reference:	MedGen: D046449 MeSH: D046449 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants