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302241000000109: Newborn blood spot screening status (finding)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Oct 2007. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module
536001000000114 Newborn blood spot screening status en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
536011000000111 Newborn blood spot screening status (finding) en Fully specified name Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Newborn blood spot screening status Is a Screening status true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Newborn blood spot screening programme - phenylketonuria (PKU) repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - congenital hypothyroidism (CHT) repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - sickle cell repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - cystic fibrosis repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - medium chain acyl-coenzyme A dehydrogenase deficiency (MCADD) repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - phenylketonuria (PKU) not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - congenital hypothyroidism (CHT) not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - sickle cell not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - cystic fibrosis not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - medium chain acyl-coenzyme A dehydrogenase deficiency (MCADD) not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, phenylketonuria not screened for or screening incomplete (finding) Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, sickle cell not screened for or screening incomplete (finding) Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, medium chain acyl-coenzyme A dehydrogenase deficiency not screened for or screening incomplete (finding) Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, cystic fibrosis not screened for or screening incomplete (finding) Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, congenital hypothyroidism not screened for or screening incomplete (finding) Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, phenylketonuria repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, cystic fibrosis repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, sickle cell repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, congenital hypothyroidism repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, medium chain acyl-coenzyme A dehydrogenase deficiency repeat screening with further sample required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, sickle cell not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, phenylketonuria not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, cystic fibrosis not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, congenital hypothyroidism not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme, medium chain acyl-coenzyme A dehydrogenase deficiency not suspected and other disorders follow up required Is a False Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - not screened for or screening incomplete Is a True Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - not suspected and other disorders follow up required Is a True Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme - repeat screening with further sample required Is a True Newborn blood spot screening status Inferred relationship Existential restriction modifier
Newborn blood spot screening programme incomplete as outside of area of current screening coverage Is a True Newborn blood spot screening status Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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