Human Phenotype Ontology 
Grandparent Node:
expandLocalized skin lesion (HP:0011355)help
Parent Node:
expandSkin plaque (HP:0200035)help
..Starting node
..expandCutaneous sclerotic plaque (HP:0031359)help
Term ID: 31359
Name: Cutaneous sclerotic plaque
Synonym:
Definition: A solid, raised, plateau-like (flat-topped) lesion greater than 1 cm in diameter that is characterized by hardening (sclerosis) of the affected skin area (related to collagen thickening).
Comments:
Reference: HP:0031359
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandErythematous plaque (HP:0025474) help
..expandUrticarial plaque (HP:0030351) help
..expandYellow skin plaque (HP:0031360) 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:0031359HP:0031359Cutaneous sclerotic plaque0 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.