Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
412881017 | Infantile hypercalcemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
412882012 | Infantile hypercalcaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
669585010 | Infantile hypercalcemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1648111000005110 | Infantil hyperkalcæmi | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Benign familiær hypercalcæmi | Is a | False | Infantile hypercalcemia | Inferred relationship | Some | |
Idiopathic infantile hypercalcaemia - mild form | Is a | False | Infantile hypercalcemia | Inferred relationship | Some | |
Severe idiopathic hypercalcemia of infancy (disorder) | Is a | False | Infantile hypercalcemia | Inferred relationship | Some | |
Idiopathic hypercalcemia of infancy | Is a | True | Infantile hypercalcemia | Inferred relationship | Some | |
A rare genetic phospho-calcic metabolism disorder characterised by early-onset hypercalcaemia, hypophosphataemia, hypercalciuria, decreased intact parathyroid hormone serum levels and medullary nephrocalcinosis, typically manifesting with failure to thrive, hypotonia, vomiting, constipation and/or polyuria. | Is a | True | Infantile hypercalcemia | Inferred relationship | Some |
Reference Sets