Human Phenotype Ontology 
Grandparent Node:
expandMorphological abnormality of the gastrointestinal tract (HP:0012718)help
Parent Node:
expandAbnormal intestine morphology (HP:0002242)help
..Starting node
..expandIntestinal lymphoid nodular hyperplasia (HP:0011956)help
Term ID: 11956
Name: Intestinal lymphoid nodular hyperplasia
Synonym:
Definition: A lymphoproliferative abnormality of the intestine characterized by numerous visible mucosal nodules measuring up to, and rarely exceeding, 0.5 cm in diameter Histologically, hyperplastic lymphoid follicles with large germinal centres are seen in the lamina propria and superficial submucosa. There is enlargement of the mucosal B cell follicles caused by hyperplasia of the follicle centres; surrounded by a normal appearing mantle zone. Disease may involve the stomach, the entire small intestine, and the large intestine.
Comments:
Reference: HP:0011956
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal large intestine morphology (HP:0002250) help
..expandAbnormality of enteric nervous system morphology (HP:0025028) help
..expandAbnormality of intestinal smooth muscle morphology (HP:0030935) help
..expandAbnormality of the small intestine (HP:0002244) help
..expandBowel diverticulosis (HP:0005222) help
..expandIntestinal atresia (HP:0011100) help
..expandIntestinal bleeding (HP:0002584) help
..expandIntestinal duplication (HP:0100668) help
..expandIntestinal edema (HP:0005225) help
..expandIntestinal fistula (HP:0100819) help
..expandIntestinal hypoplasia (HP:0005245) help
..expandIntestinal lymphangiectasia (HP:0002593) help
..expandIntestinal malrotation (HP:0002566) help
..expandIntestinal obstruction (HP:0005214) help
..expandIntestinal perforation (HP:0031368) help
..expandIntestinal polyp (HP:0005266) help
..expandIntestinal pseudo-obstruction (HP:0004389) help
..expandIntussusception (HP:0002576) help
..expandMalabsorption (HP:0002024) help
..expandMultiple intestinal neurofibromatosis (HP:0005220) help
..expandVolvulus (HP:0002580) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011956HP:0011956Intestinal lymphoid nodular hyperplasia0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.