Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire epidermis |
Is a |
True |
Epidermis structure |
Inferred relationship |
Some |
|
Stratum corneum structure |
Is a |
True |
Epidermis structure |
Inferred relationship |
Some |
|
Stratum spinosum |
Is a |
True |
Epidermis structure |
Inferred relationship |
Some |
|
Structure of dermoepidermal junction (body structure) |
Is a |
True |
Epidermis structure |
Inferred relationship |
Some |
|
Hair inner root sheath structure |
Is a |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Stratum germinativum |
Is a |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Structure of outer root sheath |
Is a |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Epidermal basement zone |
Is a |
True |
Epidermis structure |
Inferred relationship |
Some |
|
Merkel's cell |
partie de |
False |
Epidermis structure |
Additional relationship |
Some |
|
Acantholytic dyskeratotic epidermal naevus |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
4 |
Nevus striatus symmetricus of thumbs |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
4 |
Epidermal naevus syndrome |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
4 |
Epidermal antibody |
Direct substance |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Epidermal Langerhans cell |
partie de |
False |
Epidermis structure |
Additional relationship |
Some |
|
Lyell's toxic epidermal necrolysis, subepidermal type |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Linear sebaceous nevus sequence |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
4 |
Pigmented hairy epidermal nevus |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Pigmented hairy epidermal nevus |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Antibody to skin antigen measurement by immunofluorescence |
Has measured component (attribute) |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Test for Nikolsky's sign |
Procedure site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Nevus unius lateris |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
8 |
Erythema multiforme, epidermal type (disorder) |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Keratinocyte |
partie de |
False |
Epidermis structure |
Additional relationship |
Some |
|
Epidermal occlusion therapy |
Procedure site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Erythema multiforme, mixed dermal-epidermal type |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Antibody to epidermal antigen measurement |
Has measured component (attribute) |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Melanocyte |
partie de |
False |
Epidermis structure |
Additional relationship |
Some |
|
Epidermal collarette (finding) |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Hair follicle structure |
Is a |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Toxic epidermal necrolysis due to graft-versus-host disease (disorder) |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Toxic epidermal necrolysis caused by drug |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Toxic epidermal necrolysis associated with infection |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Toxic epidermal necrolysis - erythema multiforme overlap syndrome |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Stratum lucidum structure (body structure) |
Is a |
True |
Epidermis structure |
Inferred relationship |
Some |
|
Stratum granulosum |
Is a |
True |
Epidermis structure |
Inferred relationship |
Some |
|
Epidermal occlusion therapy |
Procedure site - Direct (attribute) |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Erythema multiforme, epidermal type (disorder) |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Toxic epidermal necrolysis caused by drug |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Toxic epidermal necrolysis - erythema multiforme overlap syndrome |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Epidermal occlusion therapy |
Procedure site - Direct (attribute) |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Toxic epidermal necrolysis due to graft-versus-host disease (disorder) |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Lyell's toxic epidermal necrolysis, subepidermal type |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Test for Nikolsky's sign |
Procedure site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Erythema multiforme, mixed dermal-epidermal type |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Toxic epidermal necrolysis associated with infection |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Nikolsky sign |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Superficial bacterial infection of skin |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
3 |
Structure of eyelid gland |
Is a |
False |
Epidermis structure |
Inferred relationship |
Some |
|
Epidermal fragility (finding) |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Stevens-Johnson and toxic epidermal necrolysis overlap syndrome caused by drug (disorder) |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
12 |
Severe mucocutaneous reactions; skin detachment of 10 to 30 percent of body surface area most commonly triggered by medications, characterised by extensive necrosis and detachment of the epidermis. |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
PENS syndrome is a rare, genetic, neurocutaneous syndrome characterized by the presence of randomly distributed, small, white to yellowish, multiple, rounded or irregular polycyclically-shaped, epidermal keratotic papules and plaques of gem-like appearance with a rough surface, typically located on the trunk and proximal limbs, associated with variable neurological abnormalities, including psychomotor delay, epilepsy, speech and language impairment and attention deficit-hyperactivity disorder. Clumsiness, dyslexia and ophthalmological abnormalities have also been reported. |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
A rare, genetic, epidermal disorder characterized by a chronic, diffuse, fine, scaly erythematous rash on the face (predominantly the chin, nasolabial folds, eyebrows), around the earlobes and over the scalp, associated with hyperkeratosis over elbows, knees, palms, soles and metacarpophalangeal joints, in the absence of associated rheumatological or neurological disorders. Cold weather, emotional stress and strenuous physical activity may exacerbate symptoms. |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Pemphigus foliaceus |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
Pemphigus foliaceus |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
pemphigus foliacé brésilien |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
2 |
pemphigus foliacé brésilien |
Finding site |
False |
Epidermis structure |
Inferred relationship |
Some |
1 |
Pemphigus erythematosus |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
Pemphigus erythematosus |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Drug-induced pemphigus foliaceus (disorder) |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
Drug-induced pemphigus foliaceus (disorder) |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Necrolytic migratory erythema |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
Necrolytic migratory erythema |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
Acute edema - cutaneous distension syndrome (disorder) |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
Erythema multiforme, mixed dermal-epidermal type |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |
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. |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
A rare autoimmune bullous skin disease characterized by the formation of subcorneal blisters mediated by autoantibodies against desmoglein 1, affecting predominantly seborrheic areas such as the head, neck, and upper trunk, but without any mucosal involvement. The lesions may be worsened by exposure to UV light and typically progress over weeks or months. The disease frequently occurs in children and young adults and is endemic to rural areas of Brazil and other countries in South America, as well as North Africa. |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
1 |
A rare autoimmune bullous skin disease characterized by the formation of subcorneal blisters mediated by autoantibodies against desmoglein 1, affecting predominantly seborrheic areas such as the head, neck, and upper trunk, but without any mucosal involvement. The lesions may be worsened by exposure to UV light and typically progress over weeks or months. The disease frequently occurs in children and young adults and is endemic to rural areas of Brazil and other countries in South America, as well as North Africa. |
Finding site |
True |
Epidermis structure |
Inferred relationship |
Some |
2 |