Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the lymphatic system (HP:0100763)help
Grandparent Node:
expandHamartoma (HP:0010566)help
Parent Node:
expandHamartoma of the orbital region (HP:0030670)help
Parent Node:
expandLymphangioma (HP:0100764)help
..Starting node
..expandLymphangioma of the orbit (HP:0500091)help
Term ID: 500091
Name: Lymphangioma of the orbit
Synonym:
Definition: A hamartoma of lymph vessels that usually presents in childhood. It tends to increase in size with head-down posture and with the Valsalva manoeuvre. Superficial lesions are visible as transilluminable cystic spaces of the lid or conjunctiva that may also contain blood. Deep lesions may cause gradual proptosis or present acutely with orbital pain and reduced vision due to haemorrhage.
Comments:
Reference: HP:0500091
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMediastinal cystic lymphangioma (HP:0030785) 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:0500091HP:0500091Lymphangioma of the orbit0 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.