OMOP Concept 4100490
Dysmorphic sialidosis, congenital form
StandardConditionSNOMED27642008Disorder
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 Dysmorphic sialidosis, congenital form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141619 | Dysmorphic sialidosis, congenital form | Non-standard |
| Nebraska Lexicon | 27642008 | Dysmorphic sialidosis, congenital form | Non-standard |
Synonyms
Alternative names recorded for Dysmorphic sialidosis, congenital form across source vocabularies.
- Dysmorphic sialidosis, congenital form (disorder)
- sialidosis dismórfica, forma congénita
- sialidosis dismórfica, forma congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of nervous system
- 1Developmental hereditary disorder
- 1Dysmorphic sialidosis
- 2Congenital malformation
- 2Developmental disorder
- 2Disorder of nervous system
- 2Hereditary disease
- 2Sialidosis
- 3Autosomal recessive hereditary disorder
- 3Congenital disease
- 3Disease
- 3Disorder of body system
- 3Genetic disease
- 3Inherited metabolic disorder of nervous system
- 3Mucolipidosis
- 3Myoclonic disorder
- 3Oligosaccharidosis
- 4Autosomal hereditary disorder
- 4Clinical finding
- 4Disorder of fetus and/or newborn
- 4Disorder of glycoprotein metabolism
- 4Disorder of lysosomal enzyme
- 4Hereditary disorder of nervous system
- 4Inborn error of metabolism
- 4Lysosomal storage disease
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