Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Guanosine triphosphate cyclohydrolase I deficiency (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of lysosomal enzyme |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyper-beta-alaninemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypokalemia, inadequate intake |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Xylosuria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperleucinemia (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypercalcemia due to immobilization |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cystathionine beta-synthase deficiency (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metachromatic leucodystrophy, adult type |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fructosuria (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Potassium disorder |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Primary gout |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Tennis elbow test |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal variant form of transthyretin (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Apprehension test |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ketosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal OR intrauterine hypercapnia noted before labor in liveborn infant |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autosomal recessive glutaric aciduria, type 2 |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperhydroxyprolinaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metabolic acidosis caused by methanol |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metabolic acidosis, increased anion gap (IAG) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
5-Oxoprolinase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypercalcemia caused by a drug (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of acid-base balance |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Non-amino organic acidemia AND/OR aciduria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mucopolysaccharidosis, MPS-I-H/S |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fumarylacetoacetase deficiency, acute type (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypervitaminosis D |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Maple syrup urine disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
malabsorption congénitale du glucose-galactose |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Methylene THF reductase deficiency AND homocystinuria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fructose-biphosphatase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Crigler-Najjar syndrome (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Methylmalonyl-CoA mutase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Visceral gout |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
hypovolémie |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient hyperphenylalaninaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pyridoxine dependency syndrome |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of steroid metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of sulphur-bearing amino acid metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glutaric aciduria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of porphyrin metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypervitaminosis, B complex |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypercapnia (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Combined molybdoflavoprotein enzyme deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Syndrome of carbohydrate intolerance |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Alcoholic pellagra |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dihydrolipoamide dehydrogenase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal cystine-lysinuria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Childhood hypophosphatasia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Generalized metabolic disorder |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Citrullinemia, neonatal type (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of iron metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cobalamin D disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Yergason's test (procedure) |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Thiamin-responsive maple syrup urine disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Citrullinemia, subacute type |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial hypercholesterolemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial hypokalemia-hypomagnesemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Finger-to-floor distance test |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acetyl-CoA: acyltransferase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hooft's syndrome |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Volume excess, primary hormone excess |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemodialysis-associated amyloidosis (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of purine metabolism (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydroxykynureninuria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial apolipoprotein C-II deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperornithinemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dehydration |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Idiopathic hypercalcemia of infancy |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Nonglucosuric melituria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial type 5 hyperlipoproteinemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Storage disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial hypertriglyceridemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Vitamin D deficiency (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of cobalt metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
dérèglement métabolique consécutif à une grossesse môlaire et/ou ectopique |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Iron deficiency (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypercarotinemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metabolic acidosis due to salicylate (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transfusion reaction due to excess volume (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ribose-phosphate pyrophosphokinase overactivity |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Thiamin deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperuricemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metabolic acidosis, NAG, bicarbonate losses |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aminoaciduria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Deficiency of steryl-sulfatase |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hip examination |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Disorder of the urea cycle metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Beriberi (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glutamate-cysteine ligase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypercalcemia caused by thiazide AND vitamin A |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of tyrosine metabolism (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperlipoproteinemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal hypermethioninemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of proline AND/OR hydroxyproline metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperdicarboxylicaminoaciduria AND hyperprolinaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cystathione gamma-lyase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypokalemia, excessive renal losses |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sulfite oxidase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|