Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
syndrome d'hypogonadisme hypogonadotrope-microcéphalie sévère-surdité neurosensorielle-dysmorphie |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
X-linked acrogigantism |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Leydig cell agenesis (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Familial adrenal hypoplasia with absent pituitary luteinizing hormone (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Obesity due to leptin receptor gene deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Shwachman syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Renal hepatic pancreatic dysplasia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Partial agenesis of pancreas (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Leprechaunism syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
syndrome d'insensibilité partielle aux androgènes |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Thymic, renal, anal, lung dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
pseudohypoparathyroïdie type 1A (trouble) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Congenital pancreatic enterokinase deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Pancreatic triacylglycerol lipase deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hereditary pancreatitis |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Pancreatic colipase deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
diabète sucré et diabète insipide avec atrophie optique et surdité |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
myoclonie photo-induite, diabète sucré, surdité, néphropathie et dysfonctionnement cérébral |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Diabetes-deafness syndrome maternally transmitted |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Insulin resistance - type A |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Syndrome of apparent mineralocorticoid excess |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Pseudohypoparathyroidism type 1C (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Cystic fibrosis of pancreas |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hereditary breast and ovarian cancer syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
acanthosis nigricans héréditaire bénin avec insulinorésistance |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Perilipin 1 related familial partial lipodystrophy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hyperandrogenism due to cortisone reductase deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Familial isolated hyperparathyroidism (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Familial nonmedullary thyroid carcinoma |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Diabetes mellitus co-occurrent and due to cystic fibrosis (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hereditary site-specific ovarian cancer syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
syndrome d'insuffisance hypophysaire multiple non acquise-surdité neurosensorielle-anomalies de la colonne vertébrale |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Familial infantile gigantism (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Deficiency in anterior pituitary function, variable immunodeficiency syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hypoinsulinemic hypoglycemia and body hemihypertrophy |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Corticosteroid-binding globulin deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Woodhouse Sakati syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Dyshormonogenic goitre |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
syndrome polyglandulaire auto-immun de type 1 (trouble) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Progressive cerebellar ataxia with hypogonadism |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hyperproinsulinaemia |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Ovarioleukodystrophy |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity onset diabetes of the young, type 2 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity onset diabetes of the young, type 1 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity-onset diabetes of the young, type 3 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity-onset diabetes of the young, type 5 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity-onset diabetes of the young, type 8 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity-onset diabetes of the young, type 10 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity-onset diabetes of the young, type 11 |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
X-linked panhypopituitarism (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
X-linked hypoparathyroidism (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Kallman syndrome with heart disease (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hereditary growth hormone deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Familial steroid-resistant nephrotic syndrome with adrenal insufficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
atrophie musculaire, ataxie, rétinite pigmentaire et diabète sucré |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Sanjad Sakati syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Autosomal semi-dominant severe lipodystrophic laminopathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
CIDEC-related familial partial lipodystrophy |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
LIPE-related familial partial lipodystrophy |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Peroxisome proliferator activated receptor gamma-related familial partial lipodystrophy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
AKT2-related familial partial lipodystrophy |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
4H leukodystrophy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Glucagon receptor-related hyperglucagonemia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Congenital isolated adrenocorticotropic hormone deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Inherited disorder of thyroid metabolism |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Glucocorticoid deficiency with achalasia |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Severe steroid 21-hydroxylase deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Transitory amino acid metabolic disorder |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Iodotyrosine deiodination defect |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant variant form of albumin |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Neonatal iminoglycinuria |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Maturity onset diabetes mellitus in young |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Familial adrenocortical hypoplasia |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Cholesterol monooxygenase (side-chain cleaving) deficiency |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Corticosterone 18-monooxygenase deficiency (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
17 alpha-Hydroxyprogesterone aldolase deficiency (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Testosterone 17-beta-dehydrogenase deficiency (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Transient neonatal hyperglycinaemia |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Steroid 21-monooxygenase deficiency, simple virilising type |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
3 beta-Hydroxysteroid dehydrogenase deficiency (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Moderate steroid 21-hydroxylase deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Hereditary nephrogenic diabetes insipidus |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Adrenoleukodystrophy |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Multiple endocrine neoplasia, type 3 |
est un(e) (attribut) |
True |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|
Autosomal dominant excess of transthyretin |
est un(e) (attribut) |
False |
Hereditary disorder of endocrine system (disorder) |
Inferred relationship |
Some |
|