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 |
| 9366018 | Hypophosphatemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 495555011 | Hypophosphataemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 787696012 | Hypophosphatemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypophosphatemia | Is a | Disorder of phosphate, calcium and vitamin D metabolism | false | Inferred relationship | Existential restriction modifier | ||
| Hypophosphatemia | Is a | Disorder of phosphorus metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Hypophosphatemia | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acquired hypophosphatemia | Is a | True | Hypophosphatemia | Inferred relationship | Existential restriction modifier | |
| Familial x-linked hypophosphatemic vitamin D refractory rickets | Is a | True | Hypophosphatemia | Inferred relationship | Existential restriction modifier | |
| Autosomal dominant hypophosphatemic bone disease | Is a | True | Hypophosphatemia | Inferred relationship | Existential restriction modifier | |
| Autosomal recessive hypophosphatemic bone disease | Is a | True | Hypophosphatemia | Inferred relationship | Existential restriction modifier | |
| Electrolyte management: hypophosphatemia | Has focus | True | Hypophosphatemia | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets
FHIR