Human Phenotype Ontology 
Grandparent Node:
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Telangiectasia (HP:0001009)help
Parent Node:
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Telangiectasia of the skin (HP:0100585)help
..Starting node
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Telangiectasia of extensor surfaces (HP:0007621)help
Term ID: 7621
Name: Telangiectasia of extensor surfaces
Synonym:
Definition:
Comments:
Reference: HP:0007621
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFacial telangiectasia (HP:0007380) help
..expandFingerpad telangiectases (HP:0006107) help
..expandobsolete Telangiectases in sun-exposed and nonexposed skin (HP:0007561) help
..expandPalmar telangiectasia (HP:0100869) help
..expandPeriungual teleangiectasia (HP:0025555) help
..expandPlantar telangiectasia (HP:0100870) help
..expandSpider hemangioma (HP:0012522) help
..expandTelangiectases producing 'marbled' skin (HP:0007586) help
..expandTelangiectasia of the ear (HP:0009893) 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:0007621HP:0007621Telangiectasia of extensor surfaces0SOX18 CL E G H5434511194OMIM:137940Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome.7


Genes (1) :SOX18

Diseases (1) :OMIM:137940
 

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