Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Cutaneous pythiosis (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Protothecosis of skin (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Full thickness autograft of skin to skin (procedure) |
Procedure site - Direct (attribute) |
False |
Skin structure |
Inferred relationship |
Some |
1 |
transplantation af rørformet fuldhudslap |
Procedure site - Indirect (attribute) |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Full thickness graft of skin to skin (procedure) |
Procedure site - Direct (attribute) |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Neonatal fungal infection of skin (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Xenograft of skin to skin (procedure) |
Procedure site - Direct (attribute) |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Porcine xenograft of skin to skin (procedure) |
Procedure site - Direct (attribute) |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Allograft of skin to skin (procedure) |
Procedure site - Direct (attribute) |
True |
Skin structure |
Inferred relationship |
Some |
1 |
intrabasal vesikuløs dermatit |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
intraepidermal vesikuløs dermatit |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
A rare genetic epidermal disorder with characteristics of congenital erythroderma with severe psoriasiform dermatitis, ichthyosis, severe palmoplantar keratoderma, yellow keratosis on the hands and feet, elevated immunoglobulin E, multiple food allergies, and metabolic wasting. Other variable features may include hypotrichosis, nail dystrophy, recurrent infections, mild global developmental delay, eosinophilia, nystagmus, growth impairment and cardiac defects. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
Erythroderma in infancy |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Debridement of skin graft |
Procedure site - Direct (attribute) |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Skin appendage structure |
Is a |
True |
Skin structure |
Inferred relationship |
Some |
|
Bioengineered graft of skin to skin |
Procedure site - Direct (attribute) |
True |
Skin structure |
Inferred relationship |
Some |
1 |
A rare genetic dermis elastic tissue disorder characterized by generalized cutis laxa associated with severe usually early-onset pulmonary emphysema, frequent and severe gastrointestinal and genitourinary involvement (such as bladder/intestine diverticula and/or tortuosity, gastrointestinal fragility, hydronephrosis), and mild cardiovascular involvement (typically limited to peripheral pulmonary artery stenosis only). Caused by homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
A rare genetic autoinflammatory syndrome with immune deficiency disease characterised by recurrent and severe flares of generalised pustular psoriasis associated with high fever, asthenia and systemic inflammation due to IL36R antagonist deficiency. Psoriatic nail changes (for example pitting and onychomadesis) and ichthyosis may occasionally be associated. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
A rare genetic dermis elastic tissue disease with characteristics of redundant, over folded skin of variable severity, ranging from wrinkly skin to cutis laxa associated with pre and post-natal growth retardation, hypotonia, mild to moderate developmental delay, late closure of anterior fontanelle, and craniofacial dysmorphism (including microcephaly, hypertelorism, downslanting palpebral fissures, large, prominent nasal root with funnel nose, small low-set ears, long philtrum, drooping facial skin). Additional manifestations may include seizures, intellectual disability, congenital hip dislocation, inguinal hernia and cortical and cerebellar malformations. Pretibial pseudo-ecchymotic skin lesions have occasionally been associated. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
Pustular psoriasis of sole of foot |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Pustular psoriasis of palm of hand (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Graft of skin to skin |
Procedure site - Direct (attribute) |
True |
Skin structure |
Inferred relationship |
Some |
1 |
infestation med Cheyletiella |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Dermatosis caused by Diptera |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Animal-induced dermatosis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Dermatosis caused by parasitic mammalian mite |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Arthropod dermatosis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Dermatosis caused by parasitic avian mite |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Dermatosis caused by mites (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Dermatosis due to mite infestation of stored product (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Dermatosis caused by insect mite |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Psoriasiform dermatitis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Skin infestation |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Demodex folliculitis |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Spongiotic vesicular dermatitis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Dermatophagoidal dermatosis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Kutan akarinose |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Dyremideinfestation |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Spider mite dermatitis (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Crusted scabies |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Spongiotic dermatitis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Sponge dermatitis (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Hvirveldyrsdermatose |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Hudreaktion på skadelig og/eller giftig saltvandsinvertebrate |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
A rare genetic punctate palmoplantar keratoderma disease with characteristics of discrete focal punctate keratoderma on the palms and soles and/or slowly progressive spastic paralysis, predominantly affecting the lower limbs. Lesional histology reveals pronounced orthokeratosis, acanthosis, papillomatosis, and regular undulation to the surface keratin. There have been no further descriptions in the literature since 1983. |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Epithelioid hemangioma of skin (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
Pattern bruising (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Confluent bruising |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Cystis pilonidalis uden absces |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Cystis pilonidalis med absces |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Pressure injury caused by device |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Multiple pterygium syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Lethal multiple pterygium syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
4 |
Ulcerative impetigo |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Bronchocutaneous fistula |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Nephrocutaneous fistula (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
A rare genetic developmental defect during embryogenesis syndrome with characteristics of camptodactyly, joint contractures with amyotrophy, and ectodermal anomalies (oligodontia, enamel abnormalities, longitudinally broken nails, hypohidrotic skin with tendency to excessive bruising and scarring after injuries and scratching), as well as growth retardation, kyphoscoliosis, mild facial dysmorphism and microcephaly. There have been no further descriptions in the literature since 1992. |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Benign fibromatous neoplasm of skin (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
X-linked lethal multiple pterygium syndrome is a rare, genetic, developmental defect during embryogenesis characterized by the typical lethal multiple pterygium syndrome presentation (comprising of multiple pterygia, severe arthrogryposis, cleft palate, cystic hygromata and/or fetal hydrops, skeletal abnormalities and fetal death in the 2nd or 3rd trimester) with an X-linked pattern of inheritance. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
A rare distal arthrogryposis syndrome with characteristics of multiple pterygia (typically involving the neck, axilla and popliteal areas), joint contractures, ptosis, camptodactyly of the hands with hypoplastic flexion creases, vertebral fusions, severe scoliosis and short stature. There is evidence this disease is caused by heterozygous mutation in the MYH3 gene on chromosome 17p13. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
Dermopathy due to type 2 diabetes mellitus (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Lichenoid epidermal nevus (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Diabetic dermopathy |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Diabetic thick skin syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Rubeosis faciei due to diabetes mellitus (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Hair bearing skin flap to eyebrow (procedure) |
Procedure site - Direct (attribute) |
False |
Skin structure |
Inferred relationship |
Some |
1 |
Infestation by Pyemotes ventricosus |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Lichen sclerosus of anus |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Allergic contact dermatitis of pinna (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Grocer's itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Baker's itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Copra itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Straw itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Contact dermatitis of bilateral eyelids |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Grain-shoveller's itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Hypertensivt bensår |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Ansigtseksem |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Barley itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Hypermelanosis caused by photodynamic agent (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Acute eczematoid otitis externa |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Caterpillar dermatitis (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Dermatosis caused by moth and/or butterfly |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Chronic vesicular eczema of hands (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Rottemideinfestation |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of facial dysmorphism (mild eyelid ptosis, xanthelasma, anteverted nostrils, bifid nasal tip, short palate), severe muscle wasting and cachexia, retinitis pigmentosa, numerous lentigines and cafe-au-lait spots, as well as mild soft tissue syndactyly. Additional features include nasal speech, chest asymmetry, pectus excavatum, genu varum, pes planus, and thyroid papillary carcinoma and diffuse enlargement. There has been no further description in the literature since 1984. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
Contact dermatitis caused by hydrocarbon |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Cotton-seed itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Acute-on-chronic vesicular eczema of hands and feet |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Contact dermatitis caused by acid |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Demodectic blepharitis (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Bean itch |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Syndrome with characteristics of the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular hyperpigmented dermopathy and a white forelock. It has been observed in a woman and her two daughters, whereas her son is unaffected. X-linked or autosomal dominant inheritance is proposed. |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Infestation caused by Demodex criceti (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Millipede burn (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Constitutional eczema of hands and feet |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Dermatosis caused by Echinoidea (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Acute vesicular dermatitis |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Discoid eczema of hands and feet |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Dermatoses caused by Crustacea (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Fiskelusebid |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Acute eczema (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |