Verrucae
Symptom Information:
Symptom ID: | HPO:0200043 | |||||||||||||||||||||||||||||||||||||||
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) Recurrent skin infections(HPO:0001581) Recurrent viral skin infections(HPO:0011371) Verrucae(HPO:0200043) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cutaneous neoplasms benign(MedDRA:10040899) Skin neoplasms benign(MedDRA:10040898) Verrucae(HPO:0200043) |
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Database Frequency: | 11 / 7739 | |||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Combined immunodeficiency due to STK4 deficiency | (Orphanet:314689) |
Costello syndrome | (Orphanet:3071) |
EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED | (OMIM:305350) |
Epidermodysplasia verruciformis | (Orphanet:302) |
Focal dermal hypoplasia | (Orphanet:2092) |
Immunodeficiency due to ficolin3 deficiency | (Orphanet:331190) |
KERATOSIS, SEBORRHEIC | (OMIM:182000) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
WHIM syndrome | (Orphanet:51636) |
Xeroderma pigmentosum complementation group F | (Orphanet:276264) |