Psoriasis

Symptom Information:

Symptom ID: HPO:0003765
Synonyms:
Psoriasis (disorder) [Orphanet:23250]
Psoriasis [Orphanet:23250]
Psoriasis [OMIM:Psoriasis]
Psoriasis [MedDRA:10037153]
Exacerbation of psoriasis [MedDRA:10037153]
Flexural psoriasis [MedDRA:10037153]
Other psoriasis [MedDRA:10037153]
Other psoriasis and similar disorders [MedDRA:10037153]
Psoriasis aggravated [MedDRA:10037153]
Psoriasis and similar disorders [MedDRA:10037153]
Psoriasis flare-up [MedDRA:10037153]
Psoriasis of scalp [MedDRA:10037153]
Psoriasis palm &
soles [MedDRA:10037153]
Psoriasis vulgaris [MedDRA:10037153]
Psoriatic plaque [MedDRA:10037153]
Inverse psoriasis [MedDRA:10037153]
Psoriasis facial [MedDRA:10037153]
Psoriasis genital [MedDRA:10037153]
Oral psoriasis [MedDRA:10037153]
Plaque psoriasis [MedDRA:10037153]
Non-scalp psoriasis [MedDRA:10037153]
Quality:
Cross references:
Orphanet:23250 "Psoriasis" [Orphanet:23250]
OMIM: "Psoriasis" [OMIM:Psoriasis]
UMLS:C0033860 "Psoriasis" [HPO:0003765]
UMLS:C0033860 "Psoriasis" [Orphanet:23250]
Is a (Direct Parents):
Orphanet Skin rash
HPO         Inflammatory abnormality of the skin
MedDRA Immune and associated conditions NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin physiology(HPO:0011122)
                   Inflammatory abnormality of the skin(HPO:0011123)
                      Psoriasis(HPO:0003765)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Immune disorders NEC(MedDRA:10027665)
       Immune and associated conditions NEC(MedDRA:10027682)
          Psoriasis(HPO:0003765)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V (OMIM:616100)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Bullous pemphigoid (Orphanet:703)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Cutaneous lupus erythematosus (Orphanet:535)
Generalized pustular psoriasis (Orphanet:247353)
Hemochromatosis, type 2A (OMIM:602390)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Juvenile idiopathic arthritis (Orphanet:92)
Multiple intestinal atresia (Orphanet:2300)
PSORIASIS 1, SUSCEPTIBILITY TO (OMIM:177900)
PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO (OMIM:616106)
Pemphigus erythematosus (Orphanet:79480)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
SAPHO syndrome (Orphanet:793)
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:106300)