Psoriasis
Symptom Information:
Symptom ID: | HPO:0003765 | ||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |