Papule

Symptom Information:

Symptom ID: HPO:0200034
Synonyms:
Skin papules [HPO:0200034]
Papule (morphologic abnormality) [Orphanet:23300]
Papule of skin (finding) [Orphanet:23300]
Papule (finding) [Orphanet:23300]
Papule [Orphanet:23300]
Skin Papule [Orphanet:23300]
Follicular/erythematous/edematous papules/milium [Orphanet:23300]
Papule [MedDRA:10033733]
Papule scarlet [MedDRA:10033733]
Small papule [MedDRA:10033733]
White papule [MedDRA:10033733]
Erythematous papules [Orphanet:23300]
Follicular papules [Orphanet:23300]
Follicular papule (morphologic abnormality) [Orphanet:23300]
Follicular papule [Orphanet:23300]
Follicular papules [OMIM:Follicular papules]
Edematous papules [Orphanet:23300]
Quality:
Cross references:
Orphanet:23300 "Follicular/erythematous/edematous papules/milium" [Orphanet:23300]
OMIM: "Follicular papules" [OMIM:Follicular papules]
UMLS:C0332563 "Papule" [HPO:0200034]
UMLS:C0332563 "Papule" [Orphanet:23300]
UMLS:C1519353 "Skin Papule" [Orphanet:23300]
UMLS:C0332565 "Follicular papule" [Orphanet:23300]
Is a (Direct Parents):
HPO         Hyperkeratotic papule
Orphanet Abnormality of the skin
MedDRA Dermal and epidermal conditions NEC
Orphanet Milia
HPO         Erythematous papule
HPO         Localized skin lesion
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)
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)