OMOP Concept 4180066
Gangliosidosis
StandardConditionSNOMED50967008Disorder
Maps from
15
Descendants
19
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Gangliosidosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139647 | Gangliosidosis | Non-standard |
| CIM10 | E75.1 | Other gangliosidosis | Non-standard |
| HPO | HP_0004345 | Ganglioside accumulation | Non-standard |
| ICD10 | E75.1 | Other gangliosidosis | Non-standard |
| ICD10CM | E75.1 | Other and unspecified gangliosidosis | Non-standard |
| ICD10CM | E75.10 | Unspecified gangliosidosis | Non-standard |
| ICD10CM | E75.19 | Other gangliosidosis | Non-standard |
| ICD10CN | E75.1 | Other gangliosidosis | Non-standard |
| ICD10CN | E75.100 | Other gangliosidosis | Non-standard |
| ICD10CN | E75.101 | GM3 ganglioside deposition disease (machine translation) | Non-standard |
| ICD10GM | E75.1 | Other gangliosidosis | Non-standard |
| KCD7 | E75.1 | Other gangliosidosis | Non-standard |
| MeSH | D005733 | Gangliosidoses | Non-standard |
| Read | Cyu8700 | [X]Other gangliosidosis | Non-standard |
| Read | F101400 | Gangliosidosis | Non-standard |
Synonyms
Alternative names recorded for Gangliosidosis across source vocabularies.
- acumulación de gangliósidos en lisosomas del tejido nervioso
- enfermedad por almacenamiento de gangliósidos
- Ganglioside accumulation in nervous tissue lysosomes
- Ganglioside storage disease
- gangliosidosis
- Gangliosidosis (disorder)
- gangliosidosis (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Disorder of lipid storage and metabolism
- 1Disorder of lysosomal enzyme
- 1Inherited metabolic disorder of nervous system
- 1Lysosomal storage disease
- 2Congenital disease
- 2Disorder of lipoprotein AND/OR lipid metabolism
- 2Enzymopathy
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Storage disease
- 3Disorder of nervous system
- 3Fetal and/or neonatal disorder
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 3Metabolic disease
- 4Disease
- 4Disorder of body system
- 4Hereditary disease
- 5Clinical finding
- 5Genetic disease
Narrower concepts
(19)Included automatically when you query with descendants.
- 1GM1 gangliosidosis
- 1GM2 gangliosidosis
- 2Adult chronic GM2 gangliosidosis
- 2Adult GM1 gangliosidosis
- 2Infantile GM1 gangliosidosis
- 2Infantile GM2 gangliosidosis
- 2Juvenile GM1 gangliosidosis
- 2Juvenile GM2 gangliosidosis
- 2Sandhoff disease
- 2Tay-Sachs disease
- 3B1 variant hexosaminidase A deficiency
- 3B variant hexosaminidase A deficiency
- 3Tay-Sachs disease, variant AB
- 3Total hexosaminidase deficiency - adult
- 3Total hexosaminidase deficiency - infantile
- 3Total hexosaminidase deficiency - juvenile
- 4B variant hexosaminidase A deficiency - adult
- 4B variant hexosaminidase A deficiency - infantile
- 4B variant hexosaminidase A deficiency - juvenile
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