Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of skin morphology (HP:0011121)help
Parent Node:
expandGeneralized abnormality of skin (HP:0011354)help
..Starting node
..expandGeneralized papillary lesions (HP:0007482)help
Term ID: 7482
Name: Generalized papillary lesions
Synonym: Generalised papillary lesions
Definition:
Comments:
Reference: HP:0007482
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of subcutaneous fat tissue (HP:0001001) help
..expandCutaneous photosensitivity (HP:0000992) help
..expandDermatological manifestations of systemic disorders (HP:0001005) help
..expandDesquamation of skin soon after birth (HP:0007549) help
..expandEctodermal dysplasia (HP:0000968) help
..expandFlushing (HP:0031284) help
..expandFragile skin (HP:0001030) help
..expandPoor wound healing (HP:0001058) help
..expandPrematurely aged appearance (HP:0007495) help
..expandSubcutaneous calcification (HP:0007618) help
..expandVascular skin abnormality (HP:0011276) 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:0007482HP:0007482Generalized papillary lesions0HR CL E G H558065172OMIM:209500Atrichia with papular lesions.106


Genes (1) :HR

Diseases (1) :OMIM:209500
 

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