Chronic disease
Metabolic disease
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Chronic metabolic disorder (disorder)
Chronic metabolic disorder
Chronic metabolic disease
chronische stoornis van metabolisme
chronische stofwisselingsstoornis
chronisch stofwisselingsdefect
chronische metabole stoornis
Id128289001
StatusDefined
Clinical courseChronic
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE88.9
RuleTRUE
AdviceALWAYS E88.9 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE
CorrelationSNOMED CT source code to target map code correlation not specified
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2-methyl-3-hydroxybutyric aciduria
Acute intermittent porphyria1
Acute intermittent porphyria1
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Allan-Herndon-Dudley syndrome
ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
Autosomal dominant mitochondrial myopathy with exercise intolerance
Autosomal dominant progressive external ophthalmoplegia5
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
Autosomal recessive progressive external ophthalmoplegia
Childhood-onset spasticity with hyperglycinemia
Chronic bilirubin encephalopathy
Chronic cholestatic jaundice syndrome
Chronic diarrhea with villous atrophy syndrome
Chronic gout caused by drug3
Chronic gout caused by lead2
Chronic gout without tophus2
Chronic gouty arthritis1
Chronic gouty nephropathy1
Chronic hypercapnia1
Chronic hyperglycemia
Chronic hyperkalemia
Chronic hypernatremia
Chronic hypokalemia
Chronic hyponatremia
Chronic hypoxemic respiratory failure1
Chronic milk alkali syndrome
Chronic non-neuropathic Gaucher's disease
Chronic primary gouty arthritis1
Chronic respiratory acidosis
Chronic respiratory alkalosis
Chronic tophaceous gout6
Chronic zinc deficiency
Congenital muscular dystrophy with cerebellar involvement
Congenital muscular dystrophy with intellectual disability
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Congenital muscular dystrophy without intellectual disability
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
Hemolytic anemia with emphysema AND cutis laxa
Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
Indian childhood cirrhosis
Intercritical gout
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
Larsen-like syndrome B3GAT3 type
Limb girdle muscular dystrophy due to POMK deficiency
Megaconial congenital muscular dystrophy
MEPAN syndrome
Mitochondrial neurogastrointestinal encephalomyopathy syndrome
Monoarticular chronic primary gouty arthritis
MT-ATP6-related mitochondrial spastic paraplegia
Multiple mitochondrial dysfunctions syndrome type 4
Myoclonic epilepsy with ragged red fibers
Neuronal ceroid lipofuscinosis 8
North American Indian childhood cirrhosis
Osteopetrosis with renal tubular acidosis
POGLUT1-related limb girdle muscular dystrophy R21
Polyglucosan body myopathy type 2
Progressive external ophthalmoplegia, myopathy, emaciation syndrome
Progressive intrahepatic cholestasis3
Progressive myoclonic epilepsy type 3
Progressive polyneuropathy with bilateral striatal necrosis
Progressive retinal dystrophy due to retinol transport defect
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome
Recurrent severe hypoglycemia