OMOP Concept 4208985
Hunter's syndrome, mild form
StandardConditionSNOMED5667009Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Hunter's syndrome, mild form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138396 | Hunter's syndrome, mild form | Non-standard |
| Nebraska Lexicon | 5667009 | Hunter syndrome, mild form | Non-standard |
Synonyms
Alternative names recorded for Hunter's syndrome, mild form across source vocabularies.
- Hunter's syndrome, mild form (disorder)
- Hunter syndrome, mild form
- Mucopolysaccharidosis type II mild form
- síndrome de Hunter, forma leve
- síndrome de Hunter, forma leve (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(40)Roll up to these when you need a wider cohort.
- 1Mucopolysaccharidosis, MPS-II
- 2Digestive system hereditary disorder
- 2Disorder of digestive system specific to fetus OR newborn
- 2Metabolic and genetic disorder affecting the liver
- 2Mucopolysaccharidosis
- 2X-linked recessive hereditary disease
- 3Disease of liver
- 3Disorder of digestive system
- 3Disorder of fetus and/or newborn
- 3Disorder of lysosomal enzyme
- 3Hereditary disorder by system
- 3Lysosomal storage disease
- 3Metabolic disease
- 3X-linked hereditary disease
- 4Congenital disease
- 4Digestive system finding
- 4Disease
- 4Disorder of body system
- 4Disorder of liver and/or biliary tract
- 4Enzymopathy
- 4Hereditary disease
- 4Liver finding
- 4OMOP Acute Liver Failure 1
- 4OMOP Acute Liver Failure 2
- 4OMOP Acute Liver Failure 8
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