Term ID: |
33819 |
Name: |
Perilymphatic |
Synonym: |
|
Definition: |
Applies to an abnormality whose distribution and appearance are located at or near lymphatic structures (node or vessel). |
Comments: |
|
Reference: |
HP:0033819 |
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:0033819 | HP:0033819 | Perilymphatic | 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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