Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of skin physiology (HP:0011122)help
Grandparent Node:
expand
Increased inflammatory response (HP:0012649)help
Parent Node:
expand
Inflammatory abnormality of the skin (HP:0011123)help
..Starting node
..expand
Psoriasiform dermatitis (HP:0003765)help
Term ID: 3765
Name: Psoriasiform dermatitis
Synonym: Psoriasis
Definition: A skin abnormality characterized by redness and irritation, with thick, red skin that displays flaky, silver-white patches (scales).
Comments:
Reference: HP:0003765
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcne (HP:0001061) help
..expandAtopic dermatitis (HP:0001047) help
..expandCrusting erythematous dermatitis (HP:0007473) help
..expandCutaneous abscess (HP:0031292) help
..expandDeep dermal perivascular inflammatory infiltrate (HP:0031191) help
..expandEczema (HP:0000964) help
..expandErysipelas (HP:0001055) help
..expandErythema nodosum (HP:0012219) help
..expandErythroderma (HP:0001019) help
..expandFolliculitis (HP:0025084) help
..expandNeutrophilic infiltration of the skin (HP:0031234) help
..expandPerifolliculitis (HP:0012322) help
..expandPustule (HP:0200039) help
..expandRecurrent skin infections (HP:0001581) help
..expandSkin rash (HP:0000988) help
..expandSuperficial dermal perivascular inflammatory infiltrate (HP:0031190) 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:0003765HP:0003765Psoriasiform dermatitis0ADAM17 CL E G H6868195ORPHA:294023Neonatal inflammatory skin and bowel diseaseHP:0040282 - Frequent2
HP:0003765HP:0003765Psoriasiform dermatitis0AP1S3 CL E G H13034018971OMIM:616106Psoriasis 15, pustular, susceptibility to.2
HP:0003765HP:0003765Psoriasiform dermatitis0CACNA1G CL E G H89131394ORPHA:458803Spinocerebellar ataxia type 42HP:0040283 - Occasional32
HP:0003765HP:0003765Psoriasiform dermatitis0CARD14 CL E G H7909216446OMIM:602723PSORIASIS 2; PSORS233
HP:0003765HP:0003765Psoriasiform dermatitis0CTLA4 CL E G H14932505OMIM:616100AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS510
HP:0003765HP:0003765Psoriasiform dermatitis0DSG1 CL E G H18283048OMIM:615508Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige.16
HP:0003765HP:0003765Psoriasiform dermatitis0EGFR CL E G H19563236ORPHA:294023Neonatal inflammatory skin and bowel diseaseHP:0040282 - Frequent257
HP:0003765HP:0003765Psoriasiform dermatitis0FLI1 CL E G H23133749OMIM:617443Bleeding disorder, platelet-type, 21HP:0040284 - Very rare8
HP:0003765HP:0003765Psoriasiform dermatitis0FOXP3 CL E G H509436106ORPHA:37042Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndromeHP:0040283 - Occasional32
HP:0003765HP:0003765Psoriasiform dermatitis0GATA3 CL E G H26254172ORPHA:2237Hypoparathyroidism-sensorineural deafness-renal disease syndromeHP:0040284 - Very rare83
HP:0003765HP:0003765Psoriasiform dermatitis0GJB2 CL E G H27064284ORPHA:477KID syndrome199
HP:0003765HP:0003765Psoriasiform dermatitis0GJB6 CL E G H108044288ORPHA:477KID syndrome56
HP:0003765HP:0003765Psoriasiform dermatitis0HLA-B CL E G H31064932OMIM:106300Spondyloarthropathy, susceptibility to, 1.4
HP:0003765HP:0003765Psoriasiform dermatitis0HLA-C CL E G H31074933OMIM:177900Psoriasis 1, susceptibility to.2
HP:0003765HP:0003765Psoriasiform dermatitis0HLA-DQB1 CL E G H31194944ORPHA:703Bullous pemphigoidHP:0040282 - Frequent
HP:0003765HP:0003765Psoriasiform dermatitis0HLA-DRB1 CL E G H31234948ORPHA:703Bullous pemphigoidHP:0040282 - Frequent2
HP:0003765HP:0003765Psoriasiform dermatitis0IGHG2 CL E G H35015526ORPHA:183675Recurrent infections associated with rare immunoglobulin isotypes deficiency1
HP:0003765HP:0003765Psoriasiform dermatitis0IGKC CL E G H35145716ORPHA:183675Recurrent infections associated with rare immunoglobulin isotypes deficiency5
HP:0003765HP:0003765Psoriasiform dermatitis0IL2RA CL E G H35596008OMIM:606367IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD4165
HP:0003765HP:0003765Psoriasiform dermatitis0IL36RN CL E G H2652515561OMIM:614204PSORIASIS 14, PUSTULAR; PSORS1451
HP:0003765HP:0003765Psoriasiform dermatitis0IRF2BP2 CL E G H35994821729OMIM:617765IMMUNODEFICIENCY, COMMON VARIABLE, 14; CVID144
HP:0003765HP:0003765Psoriasiform dermatitis0KNSTRN CL E G H9041730767ORPHA:221139Combined immunodeficiency with faciooculoskeletal anomaliesHP:0040282 - Frequent1
HP:0003765HP:0003765Psoriasiform dermatitis0LIG4 CL E G H39816601OMIM:606593Lig4 syndrome.88
HP:0003765HP:0003765Psoriasiform dermatitis0MSMO1 CL E G H630710545OMIM:616834Microcephaly, congenital cataract, and psoriasiform dermatitis3
HP:0003765HP:0003765Psoriasiform dermatitis0NFKB2 CL E G H47917795ORPHA:293978Deficiency in anterior pituitary function-variable immunodeficiency syndromeHP:0040283 - Occasional11
HP:0003765HP:0003765Psoriasiform dermatitis0NFKB2 CL E G H47917795OMIM:615577Immunodeficiency, common variable, 1011
HP:0003765HP:0003765Psoriasiform dermatitis0PI4KA CL E G H52978983ORPHA:436252Combined immunodeficiency-enteropathy spectrumHP:0040284 - Very rare11
HP:0003765HP:0003765Psoriasiform dermatitis0PIK3CD CL E G H52938977ORPHA:221139Combined immunodeficiency with faciooculoskeletal anomaliesHP:0040282 - Frequent9
HP:0003765HP:0003765Psoriasiform dermatitis0SLC29A3 CL E G H5531523096ORPHA:168569H syndromeHP:0040283 - Occasional68
HP:0003765HP:0003765Psoriasiform dermatitis0TP63 CL E G H862615979ORPHA:69085Limb-mammary syndromeHP:0040284 - Very rare140
HP:0003765HP:0003765Psoriasiform dermatitis0TTC7A CL E G H5721719750ORPHA:436252Combined immunodeficiency-enteropathy spectrumHP:0040284 - Very rare26
HP:0003765HP:0003765Psoriasiform dermatitis0TTC7A CL E G H5721719750OMIM:243150Gastrointestinal defects and immunodeficiency syndromeHP:0040283 - Occasional26


Genes (30) :ADAM17 AP1S3 CACNA1G CARD14 CTLA4 DSG1 EGFR FLI1 FOXP3 GATA3 GJB2 GJB6 HLA-B HLA-C HLA-DQB1 HLA-DRB1 IGHG2 IGKC IL2RA IL36RN IRF2BP2 KNSTRN LIG4 MSMO1 NFKB2 PI4KA PIK3CD SLC29A3 TP63 TTC7A

Diseases (26) :ORPHA:294023 OMIM:616106 ORPHA:458803 OMIM:602723 OMIM:616100 OMIM:615508 OMIM:617443 ORPHA:37042 ORPHA:2237 ORPHA:477 OMIM:106300 OMIM:177900 ORPHA:703 ORPHA:183675 OMIM:606367 OMIM:614204 OMIM:617765 ORPHA:221139 OMIM:606593 OMIM:616834 ORPHA:293978 OMIM:615577 ORPHA:436252 ORPHA:168569 ORPHA:69085 OMIM:243150
 

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