Human Phenotype Ontology 
Grandparent Node:
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Vascular skin abnormality (HP:0011276)help
Parent Node:
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Abnormal eyelid morphology (HP:0000492)help
Parent Node:
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Erythema (HP:0010783)help
..Starting node
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Erythema of the eyelids (HP:0040323)help
Term ID: 40323
Name: Erythema of the eyelids
Synonym: Erythema of eyelid; Eyelid erythema
Definition: Redness of the skin of the eyelids, caused by hyperemia of the capillaries in the lower layers of the skin.
Comments:
Reference: HP:0040323
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandErythema migrans (HP:0031180) help
..expandFacial erythema (HP:0001041) help
..expandNecrolytic migratory erythema (HP:0031181) help
..expandPalmoplantar erythema (HP:0025493) help
..expandShawl sign (HP:0025535) help
..expandV-sign (HP:0025536) 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:0040323HP:0040323Erythema of the eyelids0 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.