Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Phosphoenolpyruvate carboxykinase (GTP) deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperkalemia, transcellular shifts |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rowley-Rosenberg syndrome |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypervitaminosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Classical maple syrup urine disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Vitamin E deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hereditary xanthinuria (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Multiple sulfatase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of carbohydrate transport |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Starvation ketoacidosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Infantile hypophosphatasia (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ketoacidosis due to acute alcohol intoxication (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Arylsulphatase deficiency without metachromatic leucodystrophy |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hyperkalemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperlipidemia (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Essential benign pentosuria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ketoacidosis (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pellagra |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Inherited disorder of bilirubin metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypertyrosinaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pseudohypophosphatasia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Localized amyloidosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperammonemia, type III |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cholesterol ester storage disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Tyrosinosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pentose disorder |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acid phosphatase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Allen's test |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Metabolic acidosis, NAG, failure of bicarbonate regeneration |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Nutritional disorder due to calcium-phosphorus imbalance (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dihydropteridine reductase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sphingomyelin/cholesterol lipidosis (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperlysinemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial disease with storage of sterols (other than cholesterol) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pseudohypoparathyroidism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metabolic acidosis (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypokalemia, gastrointestinal losses (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperprolinemia (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metabolic acidosis caused by ethylene glycol |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Compensated acidosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Proteinosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glutamate formiminotransferase deficiency (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mucopolysaccharidosis III-B (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial hypobetalipoproteinaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Phosphate-loading hypocalcaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Iron overload (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of magnesium metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Urocanate hydratase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypocapnia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Proline dehydrogenase deficiency (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypercupremia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hypokalaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypocholesterolemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Classical galactosemia, homozygous Negro-type |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Overhydration |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Homocarnosinase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Weber's test |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital hyperammonemia, type I |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital defect of folate absorption (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Visual evoked potential study |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Uric acid level below reference range (finding) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Avian curly toe paralysis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glycine dehydrogenase (decarboxylating) deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of manganese metabolism |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Launois-Bensaude's lipomatosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Porphobilinogen synthase deficiency (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Vitamin B12 deficiency (non anemic) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
éthanolaminose |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypervitaminosis A |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperglycinemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sarcosine dehydrogenase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Electrolyte imbalance following molar AND/OR ectopic pregnancy |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Niacinamide toxicity |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Drop arm test |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Imidazole aminoaciduria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mucopolysaccharidosis, MPS-I-H |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Adenine phosphoribosyltransferase deficiency, Japanese type (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Calcinosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Persistent hyperlysinemia (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Trendelenburg test |
Procedure site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cystathioninemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Niemann-Pick disease, type C (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypercalcemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypermagnesemia (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Vitamin D intoxication |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Erythropoietic porphyria |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Wet beriberi |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cytochrome-c oxidase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Essential hypernatremia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aminomethyltransferase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Niemann-Pick disease, type C, subacute form (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Massive calcification in paraplegic |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Crigler-Najjar syndrome, type II (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sphingolipid activator protein 1 deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal OR intrauterine acidosis noted before labor in liveborn infant |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Histidine ammonia-lyase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperphenylalaninemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Tetrahydrobiopterin synthesis defect |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cystathionine gamma-lyase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Age-related amyloidosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|