OMOP Concept 4006316
Metabolic disorder of transport
StandardConditionSNOMED111394006Disorder
Maps from
1
Descendants
85
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
1 source code normalizes to Metabolic disorder of transport via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 111394006 | Metabolic disorder of transport | Non-standard |
Synonyms
Alternative names recorded for Metabolic disorder of transport across source vocabularies.
- Metabolic disorder of transport (disorder)
- metabolopatía del transporte
- trastorno del transporte metabólico
- trastorno del transporte metabólico (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(3)Roll up to these when you need a wider cohort.
Narrower concepts
(85)Included automatically when you query with descendants.
- 1Amino acid transport disorder
- 1Autosomal variant form of transthyretin
- 1Brain dopamine-serotonin vesicular transport disease
- 1Combined pancreatic lipase and colipase deficiency
- 1Disorder of oxygen transport
- 1Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome
- 1Ketoacidosis due to monocarboxylate transporter-1 deficiency
- 1Long-chain fatty acid transport deficiency
- 1Primary hypomagnesemia
- 1Progressive retinal dystrophy due to retinol transport defect
- 1Pseudohypoaldosteronism
- 1Renal tubular acidosis
- 1Secondary periodic paralysis
- 1Thyrotoxic periodic paralysis
- 1X-linked creatine deficiency
- 2Autosomal dominant primary hypomagnesemia with hypocalciuria
- 2Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
- 2Cystinemia
- 2Cystinosis
- 2Cystinuria
- 2Dicarboxylic aminoaciduria syndrome
- 2Distal renal tubular acidosis
- 2EGF-related primary hypomagnesemia with intellectual disability
- 2Familial hypomagnesemia-hypercalciuria
- 2Familial primary hypomagnesemia with normocalciuria
- 2Fanconi syndrome
- 2Gitelman syndrome
- 2Histidine transport defect
- 2Hyperkalemic renal tubular acidosis
- 2Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- 2Hypomagnesemia co-occurrent with normocalciuria
- 2Hypomagnesemia with secondary hypocalcemia
- 2Iminoglycinuria
- 2Impaired oxygen delivery
- 2Impaired oxygen extraction
- 2Increased oxygen demand
- 2Ischemic reperfusion injury
- 2Isolated autosomal dominant hypomagnesemia Glaudemans type
- 2Isolated familial intestinal hypomagnesemia
- 2Isolated familial renal hypomagnesemia
- 2Lowe syndrome
- 2Lysinuric protein intolerance
- 2Neonatal cystine-lysinuria
- 2Neutral 1 amino acid transport defect
- 2Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome
- 2Primary hypomagnesemia, refractory seizures, intellectual disability syndrome
- 2Proximal renal tubular acidosis
- 2Pseudohypoaldosteronism, type 1
- 2Pseudohypoaldosteronism, type 2
- 2Renal tubular acidosis with progressive nerve deafness
Get this concept via the API
Resolve Metabolic disorder of transport - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4006316?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card