OMOP Concept 37115758
X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency
StandardConditionSNOMED732246009Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 732246009 | X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome | Non-standard |
Synonyms
Alternative names recorded for X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency across source vocabularies.
- síndrome de discapacidad intelectual ligada al cromosoma X, espasticidad de extremidades, distrofia de retina y deficiencia de arginina vasopresina
- síndrome de discapacidad intelectual ligada al cromosoma X, espasticidad de extremidades, distrofia de retina y deficiencia de arginina vasopresina (trastorno)
- X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder)
- X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(96)Roll up to these when you need a wider cohort.
- 1Developmental hereditary disorder
- 1Disorder of purine metabolism
- 1Hereditary disorder of endocrine system
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of nervous system
- 1Hereditary vasopressin-related polyuria
- 1Leber's amaurosis
- 1Severe intellectual disability
- 1Spastic tetraparesis
- 1Vasopressin deficiency
- 1X-linked recessive hereditary disease
- 2Congenital disease
- 2Developmental disorder
- 2Disorder of endocrine system
- 2Disorder of musculoskeletal system
- 2Disorder of nervous system
- 2Disorder of posterior pituitary
- 2Disorder of purine and pyrimidine metabolism
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary retinal dystrophy
- 2Intellectual disability
- 2Spastic syndrome
- 2Tetraparesis
- 2Vasopressin-related polyuria
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