Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the fascia (HP:0100536)help
Grandparent Node:
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Increased inflammatory response (HP:0012649)help
Parent Node:
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Fasciitis (HP:0100537)help
..Starting node
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Eosinophilic fasciitis (HP:0045029)help
Term ID: 45029
Name: Eosinophilic fasciitis
Synonym:
Definition: Inflammation and thickening (localized fibrosis) of the fascia, the tissue under the skin and over the muscle, typically associated with a build up of eosinophils in the muscles and tissues.
Comments:
Reference: HP:0045029
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0045029HP:0045029Eosinophilic fasciitis0 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.