| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome d'agénésie du corps calleux-microcéphalie-petite taille | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ectodermal dysplasia with blindness syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome oro-facio-digital type 5 | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Oro-facial digital syndrome type 8 (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ackerman syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Dystrophic epidermolysis bullosa nails only (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Laryngo-onycho-cutaneous syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de kératodermie palmoplantaire-surdité | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Palmoplantar keratoderma Nagashima type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypohidrosis due to genetic abnormality of eccrine gland structure and function (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Basal epidermolysis bullosa simplex (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial multiple fibrofolliculoma (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome d'hypotrichose, lymphœdème, télangiectasie, atteinte rénale | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypotrichosis with juvenile macular degeneration syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary hypotrichosis simplex (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Macrostomia, preauricular tag, external ophthalmoplegia syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Macrocephaly, alopecia, cutis laxa, scoliosis syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Pili torti onychodysplasia syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Aplasia cutis congenita with epibulbar dermoid syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Stern Lubinsky Durrie syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypotrichosis and intellectual disability syndrome Lopes type (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Noonan syndrome-like disorder with loose anagen hair (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Recessive dystrophic epidermolysis bullosa (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal recessive aplasia cutis congenita of limb (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Trichothiodystrophy (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Transient bullous dermolysis of newborn (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Sensorineural hearing loss, early graying, essential tremor syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Keratosis follicularis, dwarfism, cerebral atrophy syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Pyogenic arthritis, pyoderma gangrenosum, acne syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| lipodystrophie partielle familiale type Köbberling | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Palmoplantar keratoderma with clinodactyly syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Junctional epidermolysis bullosa non-Herlitz type (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary hypotrichosis with recurrent skin vesicles syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Temple Baraitser syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypohidrotic X-linked ectodermal dysplasia | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Anhidrotic ectodermal dysplasia with immune deficiency (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Bullous dystrophy macular type (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial malignant melanoma of skin (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome d'ataxie cérébelleuse, déficience intellectuelle, atrophie optique, anomalies cutanées | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Genetic lipodystrophy (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary skin fragility (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Genetic disorder of skin pigmentation (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de dysplasie ectodermique-surdité neurosensorielle | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Osteopenia, intellectual disability, sparse hair syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Dermatoleukodystrophy | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary anetoderma (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Van den Bosch syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Non-androgenic hypertrichosis co-occurrent and due to genetic disease (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| epidermolyse bulleuse dystrophique dominante acrale | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| dysplasie ectodermique tricho-odonto-onychiale | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| SCARF syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| acanthosis nigricans héréditaire bénin avec insulinorésistance | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| incontinentia pigmenti | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| kératose folliculaire de Darier | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial dyskeratotic comedones | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Conductive deafness, ptosis, skeletal anomalies syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Wiedemann Steiner syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de mèches blanches et anomalies multiples | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Curly hair, acral keratoderma, caries syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| adermatoglyphie congénitale isolée | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Erythema palmare hereditarium | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome tumoral hamartomateux lié à PTEN | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Oro-facial digital syndrome type 1 (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Oro-facial digital syndrome type 14 | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Wooly hair with palmoplantar keratoderma syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial isolated trichomegaly | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Striate palmoplantar keratoderma (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Focal palmoplantar and gingival keratoderma | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Punctate palmoplantar keratoderma type 2 (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Trichoodontoonychial dysplasia | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Trichodysplasia xeroderma syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Generalized basaloid follicular hamartoma syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Upshaw-Schulman syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypertrichosis cubiti (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Alopecia, progressive neurological defect, endocrinopathy syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Leukoencephalopathy, palmoplantar keratoderma syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| dysplasie pilo-dentaire | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hidrotic ectodermal dysplasia Christianson Fourie type (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Teebi Shaltout syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Torticollis, keloids, cryptorchidism, renal dysplasia syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary progressive mucinous histiocytosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de dysplasie ectodermique-syndactylie | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  |