| 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 |
|