Human Phenotype Ontology 
Grandparent Node:
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Epidermal thickening (HP:0011368)help
Parent Node:
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Abnormality of the subungual region (HP:0009723)help
Parent Node:
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Hyperkeratosis (HP:0000962)help
..Starting node
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Subungual hyperkeratotic fragments (HP:0008410)help
Term ID: 8410
Name: Subungual hyperkeratotic fragments
Synonym:
Definition:
Comments:
Reference: HP:0008410
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCircumungual hyperkeratosis (HP:0008399) help
..expandCobblestone-like hyperkeratosis (HP:0031288) help
..expandEpidermal hyperkeratosis (HP:0007543) help
..expandFollicular hyperkeratosis (HP:0007502) help
..expandGeneralized hyperkeratosis (HP:0005595) help
..expandGingival hyperkeratosis (HP:0000222) help
..expandHyperkeratosis lenticularis perstans (HP:0007570) help
..expandHyperkeratosis over edematous areas (HP:0007448) help
..expandHyperkeratosis with erythema (HP:0007390) help
..expandHyperkeratotic papule (HP:0045059) help
..expandHyperparakeratosis (HP:0040009) help
..expandLinear arrays of macular hyperkeratoses in flexural areas (HP:0007490) help
..expandobsolete Hyperkeratosis pilaris (HP:0040180) help
..expandOrthokeratotic hyperkeratosis (HP:0025080) help
..expandPalmar hyperkeratosis (HP:0010765) help
..expandPalmoplantar keratoderma (HP:0000982) help
..expandPerifollicular hyperkeratosis (HP:0007468) help
..expandPlantar hyperkeratosis (HP:0007556) help
..expandStreaks of hyperkeratosis along each finger onto the palm (HP:0007501) help
..expandSubungual hyperkeratosis (HP:0008392) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008410HP:0008410Subungual hyperkeratotic fragments0ATP2A2 CL E G H488218ORPHA1184812108740
HP:0008410HP:0008410Subungual hyperkeratotic fragments0ATP2A2 CL E G H488218ORPHA1180812108740
HP:0008410HP:0008410Subungual hyperkeratotic fragments0ATP2A2 CL E G H488124200Keratosis follicularis124200C0022595OMIM1180812108740
HP:0008410HP:0008410Subungual hyperkeratotic fragments0ATP2A2 CL E G H488124200Keratosis follicularis124200C0022595OMIM1184812108740
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :ATP2A2

Diseases (2) :218 124200
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.