NSW Newborn Screening Service
GPTKB entity
Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:insurance
|
| gptkbp:country |
gptkb:Australia
|
| gptkbp:displayType |
gptkb:phenylketonuria
genetic disorders cystic fibrosis metabolic disorders endocrine disorders congenital hypothyroidism congenital adrenal hyperplasia galactosaemia biotinidase deficiency |
| gptkbp:founded |
1964
|
| gptkbp:headquarters |
gptkb:Sydney
|
| https://www.w3.org/2000/01/rdf-schema#label |
NSW Newborn Screening Service
|
| gptkbp:locatedIn |
gptkb:New_South_Wales
|
| gptkbp:operatedBy |
gptkb:NSW_Health_Pathology
|
| gptkbp:parentOrganization |
gptkb:NSW_Health_Pathology
|
| gptkbp:purpose |
newborn screening
|
| gptkbp:screeningMethod |
heel prick test
|
| gptkbp:serves |
gptkb:Australian_Capital_Territory
gptkb:New_South_Wales |
| gptkbp:website |
https://www.newbornscreening.health.nsw.gov.au/
|
| gptkbp:bfsParent |
gptkb:NSW_Health_Pathology
|
| gptkbp:bfsLayer |
6
|