Human Phenotype Ontology 
Grandparent Node:
expandAbnormal epidermal morphology (HP:0011124)help
Parent Node:
expandScaling skin (HP:0040189)help
..Starting node
..expandPsoriasiform lesion (HP:0025526)help
Term ID: 25526
Name: Psoriasiform lesion
Synonym: Erythemato-squamous plaque; Erythematosquamous plaque; Psoriatic-like lesion
Definition: A skin lesions that resembles the lesions observed in psoriasis, viz., an erythematous plaque covered by fine silvery scales. Psoriasiform lesions can be observed in psoriasis as well as in other conditions including allergic contact dermatitis, seborrhoeic dermatitis, Atopic dermatitis, pityriasis rubra, and lichen simplex chronicus.
Comments:
Reference: HP:0025526
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPalmoplantar scaling skin (HP:0025524) help
..expandScaling skin on fingertip (HP:0025525) help
..expandWhite scaling skin (HP:0040190) 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:0025526HP:0025526Psoriasiform lesion0CARMIL2 CL E G H14620627089OMIM:618131IMMUNODEFICIENCY 58; IMD583
HP:0025526HP:0025526Psoriasiform lesion0IL7R CL E G H35756024ORPHA:169154T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiencyHP:0040283 - Occasional94
HP:0025526HP:0025526Psoriasiform lesion0LDHA CL E G H39396535ORPHA:284426Glycogen storage disease due to lactate dehydrogenase M-subunit deficiencyHP:0040282 - Frequent35
HP:0025526HP:0025526Psoriasiform lesion0LRBA CL E G H9871742OMIM:614700IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID845


Genes (4) :CARMIL2 IL7R LDHA LRBA

Diseases (4) :OMIM:618131 ORPHA:169154 ORPHA:284426 OMIM:614700
 

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