Human Phenotype
Ontology
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Grandparent Node: Abnormality of the fascia (HP:0100536) |
Grandparent Node: Increased inflammatory response (HP:0012649) |
Parent Node: Fasciitis (HP:0100537) |
..Starting node ..Eosinophilic fasciitis (HP:0045029)
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Term ID: |
45029 |
Name: |
Eosinophilic fasciitis |
Synonym: |
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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: |
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Reference: |
HP:0045029 |
Genes and Diseases: | | Child Nodes: | Sister Nodes: | Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: | HPO disease - gene - phenotype less frequent non-typical associations: | HP:0045029 | HP:0045029 | Eosinophilic fasciitis | 0 | 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.
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