| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Facial dysmorphism, immunodeficiency, livedo, short stature syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| XTE syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome classic type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome, procollagen proteinase deficient (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome with periventricular heterotopia (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome cardiac valvular type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome kyphoscoliotic and deafness type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome, type 3 | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome musculocontractural type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos and osteogenesis imperfecta syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome kyphoscoliotic type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome vascular-like type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Brittle cornea syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Poikiloderma with neutropenia | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome spondylocheirodysplastic type | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome neurodégénératif sévère avec lipodystrophie | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Epidermolysis bullosa simplex due to exophilin 5 deficiency (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Neonatal inflammatory skin and bowel disease (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ataxia, photosensitivity, short stature syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Deafness with onychodystrophy syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial angiolipomatosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Diffuse palmoplantar keratoderma with painful fissures | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome d'Ehlers-Danlos par déficit en tenascin-X | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Skin fragility, wooly hair, palmoplantar keratoderma syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Focal palmoplantar keratoderma with joint keratoses (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Seborrhea-like dermatitis with psoriasiform elements (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Male emopamil-binding protein disorder with neurological defect | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal recessive nail dysplasia | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Inherited disorder of keratinization | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Parana hard skin syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| AGel amyloidosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Inherited cutis laxa | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ectodermal dysplasia with hair-tooth-nail-sweating defect | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Perilipin 1 related familial partial lipodystrophy (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Deficiency of interleukin 36 receptor antagonist | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Pachyonychia congenita syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Multiple pterygium syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Arthrogryposis and ectodermal dysplasia syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Inherited deformity of nail (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| porphyrie cutanée tardive familiale (trouble) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| hypoplasie dermique en aires | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary benign telangiectasia | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Odontotrichomelic syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary striate leuconychia | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de François | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Marie Unna syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary palmoplantar keratoderma | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Neonatal purpura fulminans (homozygous protein C deficiency) (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal recessive familial woolly hair | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Neurofibromatosis type 2 | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Neurofibromatosis type 1 | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Distichiasis-lymphedema syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Focal facial dermal dysplasia type I | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Focal facial dermal dysplasia type II | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Focal facial dermal dysplasia type IV (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Multiple fibrofolliculomas | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Woodhouse Sakati syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal recessive hypohidrotic ectodermal dysplasia syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Heredofamilial systemic amyloidosis affecting skin (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Poikilodermal cutaneous amyloid | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Follicular hamartoma with alopecia and cystic fibrosis syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| néphropathie amyloïde familiale avec urticaire et surdité | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary clubbing | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial lichen amyloidosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| lymphœdème héréditaire et ongles jaunes (trouble) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hyperphosphataemic familial tumoural calcinosis | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome d'Adams-Oliver (trouble) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypodontia and nail dysgenesis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Histiocytosis-lymphadenopathy plus syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Proteus syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial cutaneous collagenoma | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial spinal neurofibromatosis | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| X-linked congenital generalized hypertrichosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Infantile systemic hyalinosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Curry-Hall syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Generalized congenital lipodystrophy with myopathy (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary leiomyomatosis and renal cell carcinoma (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Tumoral calcinosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Chondrodysplasia punctata, X-linked dominant type (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Split-foot malformation, mesoaxial polydactyly syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Microcephaly, congenital cataract, psoriasiform dermatitis syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Mohr syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Orofacial-digital syndrome III | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Orofacial-digital syndrome IV | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Isolated generalized anhidrosis with normal sweat glands | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  |