OMOP Concept 438391
Amino acid transport disorder
StandardConditionSNOMED16784003Disorder
Maps from
23
Descendants
33
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
23 source codes normalize to Amino acid transport disorder via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Amino acid transport disorder across source vocabularies.
- Amino acid transport disorder (disorder)
- Disorder of amino acid transport
- trastorno del transporte de los aminoácidos
- trastorno del transporte de los aminoácidos (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(33)Included automatically when you query with descendants.
- 1Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
- 1Cystinemia
- 1Cystinosis
- 1Cystinuria
- 1Dicarboxylic aminoaciduria syndrome
- 1Fanconi syndrome
- 1Histidine transport defect
- 1Iminoglycinuria
- 1Lowe syndrome
- 1Lysinuric protein intolerance
- 1Neonatal cystine-lysinuria
- 1Neutral 1 amino acid transport defect
- 2Acquired Fanconi syndrome
- 2Adult cystinosis
- 2Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome
- 2Benign adult cystinosis
- 2Cystinuria, type 1
- 2Cystinuria, type 2
- 2Cystinuria, type 3
- 2Dibasic aminoaciduria
- 2Familial renal iminoglycinuria
- 2Hartnup disorder, renal/jejunal type
- 2Hartnup disorder, renal type
- 2Infantile nephropathic cystinosis
- 2Isolated cystinuria
- 2Juvenile nephropathic cystinosis
- 2Lysinuric protein intolerance, type 1
- 2Lysinuric protein intolerance, type 2
- 2Neonatal iminoglycinuria
- 3Adult Fanconi syndrome
- 3Atypical hypotonia cystinuria syndrome
- 3Congenital Fanconi syndrome
- 3Hypotonia cystinuria syndrome
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