Human Phenotype Ontology 
Grandparent Node:
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Epidermal thickening (HP:0011368)help
Parent Node:
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Abnormal perifollicular morphology (HP:0031285)help
Parent Node:
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Hyperkeratosis (HP:0000962)help
..Starting node
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Perifollicular hyperkeratosis (HP:0007468)help
Term ID: 7468
Name: Perifollicular hyperkeratosis
Synonym:
Definition: Increased amount of keratin (visible as white scales) surrounding hair follicles.
Comments:
Reference: HP:0007468
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
..expandPlantar hyperkeratosis (HP:0007556) help
..expandStreaks of hyperkeratosis along each finger onto the palm (HP:0007501) help
..expandSubungual hyperkeratosis (HP:0008392) help
..expandSubungual hyperkeratotic fragments (HP:0008410) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007468HP:0007468Perifollicular hyperkeratosis0HLA-DRA CL E G H3122505Acromesomelic dysplasia Campailla Martinelli typeORPHA1134947142860
HP:0007468HP:0007468Perifollicular hyperkeratosis0KRT81 CL E G H3887158000Beaded hair158000C0546966OMIM1406458602153
HP:0007468HP:0007468Perifollicular hyperkeratosis0KRT83 CL E G H3889158000Beaded hair158000C0546966OMIM11246460602765
HP:0007468HP:0007468Perifollicular hyperkeratosis0KRT83 CL E G H3889158000Beaded hair158000C0546966OMIM11236460602765
HP:0007468HP:0007468Perifollicular hyperkeratosis0KRT86 CL E G H3892158000Beaded hair158000C0546966OMIM11076463601928
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (4) :HLA-DRA KRT81 KRT83 KRT86

Diseases (2) :505 158000
 

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