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 |
|