Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the face (HP:0000271)help
Parent Node:
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Abnormality of the periorbital region (HP:0000606)help
..Starting node
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Periorbital ecchymosis with tarsal plate sparing (HP:0025553)help
Term ID: 25553
Name: Periorbital ecchymosis with tarsal plate sparing
Synonym: Raccoon eyes
Definition: Subcutaneous bleeding with a diameter greater than 1 cm (ecchymosis). The bleeding does not extend into the tarsal plate (the comparatively thick, elongated plates of dense connective tissue within the eyelid) due to an anatomic structure called the orbital septum, which limits extravasation of blood beyond the tarsal plate.
Comments:
Reference: HP:0025553
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal eyebrow morphology (HP:0000534) help
..expandAbnormal morphology of bony orbit of skull (HP:3000030) help
..expandAbnormality of the supraorbital ridges (HP:0100538) help
..expandBitemporal forceps marks (HP:0011336) help
..expandBitemporal hollowing (HP:0025386) help
..expandInfra-orbital crease (HP:0100876) help
..expandInfra-orbital fold (HP:0011232) help
..expandOrbital cyst (HP:0001144) help
..expandPeriorbital edema (HP:0100539) help
..expandPeriorbital fullness (HP:0000629) help
..expandPeriorbital hyperpigmentation (HP:0001106) help
..expandPeriorbital purpura (HP:0025552) help
..expandPeriorbital wrinkles (HP:0000607) 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:0025553HP:0025553Periorbital ecchymosis with tarsal plate sparing0 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.