Papule
Symptom Information:
Symptom ID: | HPO:0200034 | |||||||||||||||||
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) Localized skin lesion(HPO:0011355) Papule(HPO:0200034) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermal and epidermal conditions NEC(MedDRA:10012424) Papule(HPO:0200034) |
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Database Frequency: | 12 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT | (OMIM:101840) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
Generalized basaloid follicular hamartoma syndrome | (Orphanet:168632) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2 | (OMIM:616069) |
Malignant atrophic papulosis | (Orphanet:679) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE | (OMIM:616063) |
Rosaï-Dorfman disease | (Orphanet:158014) |
Sarcoidosis | (Orphanet:797) |
Tyrosinemia type 2 | (Orphanet:28378) |
Xeroderma pigmentosum complementation group F | (Orphanet:276264) |