Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 136837016 | Wolman's disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 136838014 | Primary familial xanthomatosis with adrenal calcification | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 136839018 | Familial visceral xanthomatosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 136843019 | Deficiency of cholesterol esterase AND triacylglycerol lipase | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 201017015 | Wolman xanthomatosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 201018013 | Primary familial xanthomatosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 505109013 | Wolman disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 505110015 | Acid esterase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 505111016 | Acid lipase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 823935018 | Wolman's disease (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Wolman's disease | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Wolman's disease | Is a | Disorder of lipid storage and metabolism | false | Inferred relationship | Existential restriction modifier | ||
| Wolman's disease | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Wolman's disease | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Wolman's disease | Is a | Inborn error of metabolism | false | Inferred relationship | Existential restriction modifier | ||
| Wolman's disease | Is a | Lysosomal acid lipase deficiency | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cholesterol ester storage disease | Is a | False | Wolman's disease | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR