Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
A rare punctate palmoplantar keratoderma characterized by multiple small, round to oval or rhomboid, yellowish, hyperkeratotic papules and plaques most commonly localized to the palms of the hands and soles of the feet, potentially extending to the dorsum of the hands and feet in severe cases. Histopathological analysis shows hyperkeratosis, epidermal hypertrophy, and fragmentation and rarefaction of elastic fibers. The condition can be sporadic or familial. |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Dermatosis papulosa nigra |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Granulosis rubra nasi |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
Painful piezogenic pedal papules |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Keratosis pilaris |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
Initial lesion of yaws |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Erythromelanosis follicularis of face AND/OR neck |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Urticaria pigmentosa, maculopapular type |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
Viral papular dermatitis |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
Acquired keratosis pilaris |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
Papular yaws |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Atrophoderma vermiculatum (disorder) |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Pruritic folliculitis of pregnancy |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Gianotti-Crosti syndrome |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
Painful pigmented pressure papules |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Hereditary acrodermatitis enteropathica |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
No papule of skin |
Associated finding |
True |
Papule of skin |
Inferred relationship |
Some |
1 |
Acne varioliformis |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Papular eruption |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Maculopapular eruption |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Maculopapular sarcoidosis |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Micropapular wheal |
Is a |
False |
Papule of skin |
Inferred relationship |
Some |
|
A rare, acquired, dermis elastic tissue disorder characterized by multiple, asymptomatic, firm, well-demarcated, nonfollicular, hypopigmented or skin-colored papules, with a diameter of less than 1 cm, distributed symmetrically over trunk and/or proximal limbs (rarely, head, neck, shoulders, armpits, thighs), with no extracutaneous manifestations. Histopathology typically reveals decreased and fragmented elastic fibers, thickened and/or homogenized collagen bundles and, in some, a mild, perivascular, lymphocytic infiltrate in the dermis. |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
Infantile pedal papules |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|
A form of cutaneous mastocytosis (CM) characterised by the presence of multiple hyperpigmented macules, papules or nodules associated with abnormal accumulation of mast cells in the skin. Most patients present in infancy or childhood, but onset may also occur in adulthood. Mutations in the KIT gene (4q11-q12) have been identified however this mutation is rare in the paediatric population and the aetiology and pathogenesis in these cases remains to be determined. The disease generally occurs sporadically but rare familial cases have been reported. |
Is a |
True |
Papule of skin |
Inferred relationship |
Some |
|