Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
A rare autoinflammatory syndrome with characteristics of the presence of features of relapsing polychondritis and Behcet disease in the same individual. This includes cartilage inflammation of the ears, nose, throat and rib cage as well as recurrent oral and genital ulcers respectively. Patients may also present ocular involvement (in particular anterior uveitis or scleritis), arthritis, fever, colitis, thrombophlebitis, and central nervous system vasculitis or in rare cases arterial aneurysms. Symptoms of polychondritis occur secondary to those of Behcet disease in the vast majority of cases. |
Is a |
False |
Collagen and elastic tissue disorders affecting skin |
Inferred relationship |
Some |
|
Extensive congenital erosions, vesicles and reticulate scarring (disorder) |
Is a |
True |
Collagen and elastic tissue disorders affecting skin |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome |
Is a |
False |
Collagen and elastic tissue disorders affecting skin |
Inferred relationship |
Some |
|
Menkes kinky-hair syndrome |
Is a |
True |
Collagen and elastic tissue disorders affecting skin |
Inferred relationship |
Some |
|
Cutis laxa |
Is a |
True |
Collagen and elastic tissue disorders affecting skin |
Inferred relationship |
Some |
|
A rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs. |
Is a |
True |
Collagen and elastic tissue disorders affecting skin |
Inferred relationship |
Some |
|
A rare, acquired, dermis elastic tissue disorder with decreased elastic tissue characterized by multiple, asymptomatic, well demarcated, flat, hypopigmented atrophic macular skin lesions distributed over upper trunk and proximal upper limbs. Histopathological examination reveals atrophic epidermis with decreased basal pigmentation, perivascular mononuclear infiltration in the upper dermis, and disorganized, hyalinized, coarse collagen bundles, and variable loss of elastic fibers in the dermis. |
Is a |
True |
Collagen and elastic tissue disorders affecting 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 |
Collagen and elastic tissue disorders affecting skin |
Inferred relationship |
Some |
|