Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
arthrogrypose-hyperkératose létale |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Macrostomia, preauricular tag, external ophthalmoplegia syndrome (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Van den Bosch syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital alopecia with keratin cysts |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
porokératose actinique superficielle disséminée |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
syndrome d'agénésie du corps calleux-microcéphalie-petite taille |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
maladie de Rendu-Osler |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Wooly hair with palmoplantar keratoderma syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Palmoplantar keratoderma with clinodactyly syndrome (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Hereditary benign intraepithelial dyskeratosis (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Porokeratosis of Mibelli, linear unilateral type |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Porokeratosis of Mibelli, superficial disseminated type |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Porokeratosis of Mibelli, plaque type |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital erosive and vesicular dermatosis |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
syndrome de dermatite sévère-allergies multiples-cachexie métabolique |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Median raphe cyst (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Male emopamil-binding protein disorder with neurological defect |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Macrocephaly, alopecia, cutis laxa, scoliosis syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Autosomal recessive cutis laxa type 2B |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Localized abdominal wall skin atrophy |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Multiple pterygium syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital diffuse lipomatosis |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Encephalocraniocutaneous lipomatosis |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Leprechaunism syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
syndrome de François |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Cutis laxa, x-linked (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Erythrokeratodermia variabilis |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital hypertrophy of lateral fold of hallux |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital malalignment of great toenail (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Blepharophimosis epicanthus inversus ptosis syndrome plus (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Wrinkly skin syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Pulmonary tuberous sclerosis (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Ash leaf spot, tuberous sclerosis |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
polykystose rénale autosomique dominante type 1 avec sclérose tubéreuse |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital extramedullary dermal hematopoiesis |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
défaut d'alignement congénital de multiples ongles d'orteil (trouble) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Blepharophimosis epicanthus inversus ptosis syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital cutaneous lymphangiectasia |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Hooded penis |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Mandibuloacral dysostosis |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital commissural pits |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Lip pits |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Patent urachal duct |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Genitoperineal raphe cyst |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Lumpy scalp syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
ichtyose congénitale |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
phimosis congénital |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Short preputial frenulum |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Geroderma osteodysplastica |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital vascular naevus |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Cavernous lymphangioma of skin |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Cyanotic congenital heart disease |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Preauricular cyst |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Nail-patella syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Goltz syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Cervical auricle |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital hyperplasia of sebaceous glands of lip |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Accessory tragus of ear |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Patent urachus |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
prépuce redondant |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
angiodysplasie ostéodystrophique |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Dermatofibrosis lenticularis disseminata |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital oculocutaneous hypopigmentation |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Hajdu-Cheney syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Nevus unius lateris |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Pilonidal cyst without abscess |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Pilonidal cyst with abscess |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital melanosis (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Capillary fragility abnormality |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
anomalies congénitales de pigmentation de la peau |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital deficiency of pigment of skin |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Fistula of congenital auricle |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Synophrys |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Absent eyebrow |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Double eyebrow |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
anomalie congénitale de l'ongle (trouble) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
incontinentia pigmenti |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Naevus anaemicus |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Mixed haemangioma |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Unilateral segmental cavernous hemangioma (situation) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Verrucous hemangioma of skin |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
ostéolyse massive idiopathique |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Angiokeratoma circumscriptum |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Cutis marmorata (finding) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Congenital skin fragility of animals |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Nevus comedonicus |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
angiome serpigineux |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
syndrome de Werner (trouble) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Ataxia-telangiectasia syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Patent urachus (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Fistula of urachus (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|
Deep hemangioma of skin (disorder) |
est un(e) (attribut) |
False |
Congenital anomaly of skin |
Inferred relationship |
Some |
|