Human Phenotype Ontology 
Grandparent Node:
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Vascular neoplasm (HP:0100742)help
Parent Node:
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Hemangioma (HP:0001028)help
..Starting node
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Glabellar hemangioma (HP:0001076)help
Term ID: 1076
Name: Glabellar hemangioma
Synonym: Glabellar capillary hemangioma
Definition:
Comments:
Reference: HP:0001076
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandArachnoid hemangiomatosis (HP:0012222) help
..expandCapillary hemangioma (HP:0005306) help
..expandCardiac hemangioma (HP:0011673) help
..expandCavernous hemangioma (HP:0001048) help
..expandChoroidal hemangioma (HP:0007872) help
..expandFacial hemangioma (HP:0000329) help
..expandGlomeruloid hemangioma (HP:0031357) help
..expandHemangiomatosis (HP:0007461) help
..expandHepatic hemangioma (HP:0031207) help
..expandPerineal hemangioma (HP:0031449) help
..expandRetinal capillary hemangioma (HP:0009711) help
..expandTufted angioma (HP:0012329) 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:0001076HP:0001076Glabellar hemangioma0RRAS2 CL E G H2280017271OMIM:618624NOONAN SYNDROME 12; NS121
HP:0001076HP:0001076Glabellar hemangioma0SLC26A2 CL E G H183610994OMIM:222600Diastrophic dysplasia.166
HP:0001076HP:0001076Glabellar hemangioma0TBX2 CL E G H690911597OMIM:618223VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION.


Genes (3) :RRAS2 SLC26A2 TBX2

Diseases (3) :OMIM:618624 OMIM:222600 OMIM:618223
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.