Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the nail (HP:0001597)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Abnormality of the periungual region (HP:0100803)help
Parent Node:
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Fibroma (HP:0010614)help
Parent Node:
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Neoplasm of the nail (HP:0100826)help
..Starting node
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Ungual fibroma (HP:0100804)help
Term ID: 100804
Name: Ungual fibroma
Synonym: Koenen tumor; Koenen tumour; Koenen's tumor; Koenen's tumour; Parungual fibromas; Periungual fibroma
Definition: Flesh-colored papule in or around the nail bed. Ungual fibromas may be periungual (arising under the proximal nail fold) or subungual (originating under the nail plate).
Comments:
Reference: HP:0100804
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100804HP:0100804Ungual fibroma0IFNG CL E G H34585438ORPHA:805Tuberous sclerosis complexHP:0040283 - Occasional23
HP:0100804HP:0100804Ungual fibroma0TSC1 CL E G H724812362ORPHA:538LymphangioleiomyomatosisHP:0040282 - Frequent1090
HP:0100804HP:0100804Ungual fibroma0TSC1 CL E G H724812362ORPHA:805Tuberous sclerosis complexHP:0040283 - Occasional1090
HP:0100804HP:0100804Ungual fibroma0TSC2 CL E G H724912363ORPHA:538LymphangioleiomyomatosisHP:0040282 - Frequent2738
HP:0100804HP:0100804Ungual fibroma0TSC2 CL E G H724912363ORPHA:805Tuberous sclerosis complexHP:0040283 - Occasional2738


Genes (3) :IFNG TSC1 TSC2

Diseases (2) :ORPHA:805 ORPHA:538
 

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