| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Chronic hypokalemia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Urate nephropathy | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic hypernatremia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic anoxic encephalopathy | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic hyperkalemia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic hyponatremia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic milk alkali syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Hemolytic anemia with emphysema AND cutis laxa | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic non-neuropathic Gaucher's disease | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic arthritis due to gout | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic zinc deficiency | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Hepatogenous chronic copper poisoning | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic tophaceous gout | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic cholestatic jaundice syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic hypertensive uremia | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic respiratory acidosis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital hypoplastic anemia | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic respiratory alkalosis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic hyperglycemia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic urate nephropathy | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Acute intermittent porphyria | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Saturnine nephropathy | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Benign recurrent intrahepatic cholestasis | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Recurrent severe hypoglycemia | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Hepatic coma due to chronic hepatitis B | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic hypoxemic respiratory failure | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic hypercapnia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic gout without tophus | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Lichen amyloidosis | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic primary gouty arthritis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic diarrhea with villous atrophy syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic painful neuropathy due to diabetes mellitus | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Indian childhood cirrhosis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Myoclonic epilepsy with ragged red fibers | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Progressive polyneuropathy with bilateral striatal necrosis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Childhood-onset spasticity with hyperglycinemia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Progressive retinal dystrophy due to retinol transport defect | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Progressive myoclonic epilepsy type 3 | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Familial dementia British type | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital muscular dystrophy with intellectual disability | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital muscular dystrophy without intellectual disability | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital muscular dystrophy with cerebellar involvement | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital muscular dystrophy with intellectual disability and severe epilepsy | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Familial dementia Danish type | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Osteopetrosis with renal tubular acidosis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Reunion Island Larsen-like syndrome | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic tophaceous gout of shoulder caused by drug | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| North American Indian childhood cirrhosis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Mitochondrial neurogastrointestinal encephalomyopathy syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Progressive external ophthalmoplegia, myopathy, emaciation syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Autosomal dominant progressive external ophthalmoplegia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Autosomal recessive progressive external ophthalmoplegia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Progressive epilepsy-intellectual disability syndrome Finnish type | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Intercritical gout | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic gout caused by drug | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Chronic gout caused by lead | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Monoarticular chronic primary gouty arthritis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Progressive intrahepatic cholestasis | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| 2-methyl-3-hydroxybutyric aciduria | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Monocarboxylate transporter 8 deficiency | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Kernicterus spectrum disorder | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Multiple mitochondrial dysfunctions syndrome type 4 | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Autosomal dominant mitochondrial myopathy with exercise intolerance | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Polyglucosan body myopathy type 2 | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Megaconial congenital muscular dystrophy | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Classical-like Ehlers-Danlos syndrome type 2 | Is a | False | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  | 
| Spastic ataxia, dysarthria due to glutaminase deficiency | Is a | True | Chronic metabolic disorder | Inferred relationship | Existential restriction modifier |  |