| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Isolated generalized anhidrosis with normal sweat glands | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Juvenile hyaline fibromatosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Peroxisome proliferator activated receptor gamma-related familial partial lipodystrophy (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| AKT2-related familial partial lipodystrophy | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal semi-dominant severe lipodystrophic laminopathy (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| CIDEC-related familial partial lipodystrophy | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| LIPE-related familial partial lipodystrophy | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| LAMA5-related multisystemic syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial chilblain lupus erythematosus (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial multiple discoid fibroma | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| ichtyose congénitale | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial chronic mucocutaneous candidiasis - dominant type | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial chronic mucocutaneous candidiasis - recessive type | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Fabry's disease | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Nail-patella syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Cholestanol storage disease | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Sitosterolemia with xanthomatosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| acro-céphalo-syndactylie de type V | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal dominant mutilating keratoderma | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Albinism | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Progeria syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial Mediterranean fever | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Giacci familial neurogenic acroosteolysis (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de Wiskott-Aldrich (trouble) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| acrodermatite entéropathique héréditaire (trouble) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Lipid proteinosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| syndrome de Papillon-Lefèvre (trouble) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| xeroderma pigmentosum | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| pseudoporphyrie médicamenteuse | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial multiple polyposis syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Premature aging syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary benign intraepithelial dyskeratosis (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Pseudoporphyria due to PUVA therapy | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Porphyria-like reaction to poison and/or environmental toxin | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary neurocutaneous angiomata (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| cutis laxa | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Menkes kinky-hair syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial acantholysis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Epidermolysis bullosa | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Porphyria cutanea tarda | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Xanthomatosis | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Cutis laxa, autosomal dominant | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Cutis laxa, autosomal recessive (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal dominant epidermolysis bullosa simplex (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary benign intraepithelial dyskeratosis | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Gorlin syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary coproporphyria | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hypopigmentation-immunodeficiency disease | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ocular albinism-lentigines-deafness syndrome (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| albinoïdisme | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Oculocutaneous albinism | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary edema of legs | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hemodialysis-associated pseudoporphyria (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Klein-Waardenberg's syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal dominant hypohidrotic ectodermal dysplasia syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Neurocutaneous syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Reticulate acropigmentation of Kitamura | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Multiple lentigines syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Pili torti-deafness syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ataxia-telangiectasia syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Farber's lipogranulomatosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary angioedema | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| stéatocystomes multiples | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Familial cold urticaria | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Pachydermoperiostosis syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Mandibuloacral dysostosis | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| maladie de Rendu-Osler | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Marfan's syndrome affecting skin | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Ultraviolet sensitive syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Severe achondrolasia with developmental delay and acanthosis nigricans (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Dyskeratosis congenita | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Follicular atrophoderma and basal cell epitheliomata | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Multiple self-healing epithelioma of Ferguson-Smith | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| b-K mole syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Schinzel-Giedion syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Rothmund-Thomson syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Crouzon syndrome with acanthosis nigricans (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Kohlschutter's syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Autosomal dominant familial woolly hair | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| porokératose superficielle disséminée | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| maladie de von Hippel-Lindau (trouble) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary neurocutaneous angiomata (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| lentiginose périorificielle avec polypose viscérale | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Tuberous sclerosis syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Neurofibromatosis syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Congenital reticular ichthyosiform erythroderma (disorder) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Cutis gyrata syndrome of Beare and Stevenson | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Brooke-Spiegler syndrome | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Capillary malformation-arteriovenous malformation syndrome (disorder) | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Legius syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Hereditary sclerosing poikiloderma | est un(e) (attribut) | True | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Acral peeling skin syndrome | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| atrophodermie vermiculée (trouble) | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  | 
| Cole disease | est un(e) (attribut) | False | Hereditary disorder of the integument | Inferred relationship | Some |  |