Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the face (HP:0000271)help
Parent Node:
expandAbnormality of the periorbital region (HP:0000606)help
..Starting node
..expandPeriorbital purpura (HP:0025552)help
Term ID: 25552
Name: Periorbital purpura
Synonym:
Definition: Multiple red/purple spots on the skin that surrounds the eyes that do not blanch (whiten) upon pressure. Purpura is caused by subcutaneous bleeding.
Comments:
Reference: HP:0025552
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 ecchymosis with tarsal plate sparing (HP:0025553) help
..expandPeriorbital edema (HP:0100539) help
..expandPeriorbital fullness (HP:0000629) help
..expandPeriorbital hyperpigmentation (HP:0001106) 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:0025552HP:0025552Periorbital purpura0 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.