Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Urate nephropathy |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute neuronopathic Gaucher's disease (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute cholestatic jaundice syndrome (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute zinc deficiency |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fumarylacetoacetase deficiency, acute type (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hyponatremia |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
syndrome d'urémie prérénale |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hyperkalemia |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute respiratory alkalosis |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hypokalaemia |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial arthrogryposis-cholestatic hepatorenal syndrome |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute respiratory acidosis (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hypernatremia (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute mountain sickness |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute milk alkali syndrome |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute neuronopathic Gaucher's disease (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transitory neonatal electrolyte disturbance |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transitory amino acid metabolic disorder |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute zinc deficiency |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute urate nephropathy |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hyperglycemia |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
syndrome d'urémie prérénale |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial arthrogryposis-cholestatic hepatorenal syndrome |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute respiratory acidosis (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute milk alkali syndrome |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transitory neonatal diabetes mellitus (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal bullous dermatosis |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal hyperglycaemia |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Idiopathic transient neonatal hyperinsulinemia (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hepatic coma due to acute hepatitis B (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transitory neonatal hypoglycemia (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal renal tubular acidosis |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal hyperglycinemia |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal hypertyrosinemia |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hepatic coma due to acute hepatitis B with delta agent (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal multiple acyl-CoA dehydrogenase deficiency describes a very rare condition where a maternal riboflavin deficiency causes an infant to present with manifestations similar to those seen in multiple acyl-CoA dehydrogenase (MAD) deficiency such as poor suck, metabolic acidosis and hypoglycemia, but that resolves completely with oral riboflavin. In the one patient described haploinsufficiency of the human riboflavin transporter (hRFT1) was described in the mother. |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient bullous dermolysis of newborn (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transitory metabolic disturbance in infant of pre-diabetic mother (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute pericarditis co-occurrent and due to uremia (disorder) |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute complication due to diabetes mellitus |
Is a |
False |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hypoxemic respiratory failure (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute hypercapnic respiratory failure |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute gout |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient infantile hypertriglyceridemia and hepatosteatosis |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Thyrotoxicosis due to acute thyroiditis |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dialysis disequilibrium syndrome |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare neurologic disease characterized by lethargy, hypotonia, poor feeding, opisthotonus, and a typical high-pitched cry due to bilirubin accumulation in the globus pallidus, sub-thalamic nuclei, and other brain regions, resulting from severe neonatal unconjugated hyperbilirubinemia. Onset of symptoms is typically within the first three to five days of life. Additional features include fever, apnea, seizures, and coma. Respiratory failure or refractory seizures may lead to a fatal outcome. |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal transient metabolic disturbance (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Porphyria-induced phototoxic burn (disorder) |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare neurometabolic disease characterized by acute, reversible, and sometimes recurrent neurologic deterioration (including drowsiness, hypotonia, dysarthria, and ataxia) during a febrile illness. The condition is associated with reversible leukoencephalopathy and persistently increased urinary excretion (and sometimes cerebrospinal fluid concentration) mainly of alpha-ketoglutarate and N-acetylaspartate. |
Is a |
True |
Acute metabolic disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|