Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandDigestive System Abnormalities (D004065)
Parent Node:
expandDiverticulum (D004240)
..Starting node
..expandMeckel Diverticulum (D008467)

       Child Nodes:



 Sister Nodes: 
..expandBladder Diverticulum (C562406)
..expandDiverticulosis, Small Intestinal (C565620)
..expandDiverticulum, Colon (D004241)
..expandDiverticulum, Esophageal (D004936) Child1
..expandDiverticulum, Stomach (D013273)
..expandMeckel Diverticulum (D008467)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6859
Name:Meckel Diverticulum
Definition:A congenital abnormality characterized by the outpouching or sac formation in the ILEUM. It is a remnant of the embryonic YOLK SAC in which the VITELLINE DUCT failed to close.
Alternative IDs:
ParentIDs:MESH:D004065|MESH:D004240
TreeNumbers:C06.198.859 |C16.131.314.556 |C23.300.415.750
Synonyms:Diverticulum, Meckel |Meckel's Diverticulum
Slim Mappings:Congenital abnormality|Digestive system disease|Pathology (anatomical condition)
Reference: MedGen: D008467
MeSH: D008467
OMIM: 155140;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0002245Meckel diverticulum
Disease Causing ClinVar Variants