Human Phenotype Ontology 
Grandparent Node:
expandAbnormal macrophage morphology (HP:0004311)help
Parent Node:
expandGranulomatosis (HP:0002955)help
..Starting node
..expandNon-caseating epithelioid cell granulomatosis (HP:0012220)help
Term ID: 12220
Name: Non-caseating epithelioid cell granulomatosis
Synonym:
Definition: The presence of multiple epithelioid cell granulomas consist of highly differentiated mononuclear phagocytes (epithelioid cells and giant cells) and lymphocytes, not exhibiting caseation (a form of necrosis in which the tissue changes into a dry, amorphous mass said to resemble cheese).
Comments:
Reference: HP:0012220
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCerebral granulomatosis (HP:0100313) help
..expandHepatic granulomatosis (HP:0011955) help
..expandLipogranulomatosis (HP:0040139) 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:0012220HP:0012220Non-caseating epithelioid cell granulomatosis0 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.