Human Phenotype Ontology 
Grandparent Node:
expandAbnormal macrophage morphology (HP:0004311)help
Parent Node:
expandAbnormal cerebral morphology (HP:0002060)help
Parent Node:
expandGranulomatosis (HP:0002955)help
..Starting node
..expandCerebral granulomatosis (HP:0100313)help
Term ID: 100313
Name: Cerebral granulomatosis
Synonym:
Definition: Cerebral inflammation involving a granulomatous response, i.e., a non-specific inflammatory response involving granulomas, defined as a compact organized collection of mature mononuclear phagocytes including epithelioid and giant cells.
Comments:
Reference: HP:0100313
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHepatic granulomatosis (HP:0011955) help
..expandLipogranulomatosis (HP:0040139) help
..expandNon-caseating epithelioid cell granulomatosis (HP:0012220) 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:0100313HP:0100313Cerebral 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.