Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Alstrom syndrome |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Inborn error of metabolism |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Inherited methylmalonic acidaemia AND homocystinuria |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary xanthinuria |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Citrullinemia (disorder) |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Inherited disorder of porphyrin metabolism (disorder) |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Familial benign copper deficiency |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary hemochromatosis |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Autosomal dominant beta2-microglobulinic amyloidosis (disorder) |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary hypertyrosinemia |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Inherited aminoaciduria |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Thymidine kinase 2 deficiency |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Leukodystrophy due to alkaline ceramidase 3 deficiency (disorder) |
Is a |
True |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
2-hydroxyglutaric aciduria |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary fructosuria |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Deficiency of phosphomannomutase 2 (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Tyrosinemia type III (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Epidermolysis bullosa simplex with pyloric atresia |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Deficiency of steroid 17-alpha-monooxygenase |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
hereditaire sideroblastische anemie |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Autosomal dominant beta2-microglobulinic amyloidosis (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Familial hypertryptophanemia (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hyperprolinemia type 2 (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Virilisation-adrenogenital syndrome |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Homocystinuria without methylmalonic aciduria (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
X-linked creatine deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Lesch-Nyhan syndrome |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hawkinsinuria (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Dihydropyrimidine dehydrogenase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary cerebral amyloid angiopathy, Icelandic type |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Late-onset junctional epidermolysis bullosa (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Isolated hyperchlorhidrosis (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Placental sulfatase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Tyrosinemia type I (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Autosomal recessive hypophosphatemic bone disease |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Autosomal dominant epidermolysis bullosa simplex (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Familial amyloid polyneuropathy (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Childhood myocerebrohepatopathy spectrum (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Juvenile cataract, microcornea, renal glucosuria syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Familial Mediterranean fever |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Congenital bile acid synthesis defect type 3 (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Sucrase-isomaltase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hepatic lipase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hyperinsulinism due to deficiency of glucokinase (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Adenosine deaminase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary acrodermatitis enteropathica |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Bartter syndrome type 4a (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hyperuricemia, anemia, renal failure syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Deficiency of steroid 11-beta-monooxygenase |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Beta-aminoisobutyric aciduria (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Deficiency of leukotriene C4 synthase (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Essential benign fructosuria |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary cerebral amyloid angiopathy, Dutch type |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Familial hypokalemic alkalosis, Gullner type |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Cytochrome P450 oxidoreductase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Inherited aminoaciduria |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Autosomal dominant optic atrophy plus syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Homogentisate 1,2-dioxygenase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hyperinsulinism and hyperammonemia syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Congenital lactase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Severe X-linked mitochondrial encephalomyopathy (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Congenital analbuminemia (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Alstrom syndrome |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Lipid proteinosis |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Wilson's disease |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Orotic aciduria |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hypotonia cystinuria syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Deficiency of AMP pyrophorylase |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hypomagnesemia with secondary hypocalcemia (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
syndroom van epilepsie, ataxie, perceptief gehoorverlies en tubulopathie (aandoening) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Deficiency of phosphoserine aminotransferase (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Basal epidermolysis bullosa simplex (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Deficiency of dimethylglycine dehydrogenase (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Zellweger-like syndrome without peroxisomal anomaly (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hereditary oculoleptomeningeal amyloid angiopathy |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
3-Methylglutaconic aciduria type 1 |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Laryngo-onycho-cutaneous syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Dystrophic epidermolysis bullosa nails only (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Purine-nucleoside phosphorylase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
geïsoleerde xanthineoxidasedeficiëntie |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Glucose transporter protein type 1 deficiency syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Transcobalamin II deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
MEHMO syndrome |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Pseudohypoparathyroidism type 1C (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
3-Methylglutaconic aciduria type 2 |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Adenylosuccinate lyase deficiency |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Lathosterolosis (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hypomagnesemia co-occurrent with normocalciuria (disorder) |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|
Hyperphosphatasaemia with intellectual disability |
Is a |
False |
Hereditary metabolic disease |
Inferred relationship |
Some |
|