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1244621000168103: Australian emergency department reference set (foundation metadata concept)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module
3194481000168117 Australian emergency department reference set (foundation metadata concept) en Fully specified name Active Case sensitive SNOMED Clinical Terms Australian extension
3194491000168119 Australian emergency department reference set en Synonym Active Case sensitive SNOMED Clinical Terms Australian extension
3194501000168114 Australian EDRS (emergency department reference set) en Synonym Active Case sensitive SNOMED Clinical Terms Australian extension
4351711000168117 <p>Supports the recording of reasons for presentation, presenting problems and diagnoses within emergency department settings in Australia.&nbsp;</p><p>It supersedes and expands on the content of the earlier Emergency Department Reference Set (EDRS) suite to provide a wide range of clinically relevant terms to enable safe clinical care delivery, a capability to serve clinician decision support, care guidelines and pathways, and provide interoperability with inpatient and general practice records when patients transferred between care settings.</p><p>This reference set supports the accurate and unambiguous electronic communication and exchange of information between clinicians involved in a patient's care relating to that patient's presentation at the point of triage and diagnosis at the point of discharge from an Emergency department.</p><p><b>Target client: </b>NCTS</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


90032 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Australian emergency department reference set Is a Emergency department clinical group true Inferred relationship Some
Australian emergency department reference set Is a Simple type reference set true Inferred relationship Some
Australian emergency department reference set Developed by Australian Digital Health Agency true Inferred relationship Some 1937751348
Australian emergency department reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1188790823

Members
X chromosome-linked pyridoxine responsive sideroblastic anaemia
X chromosome-linked sideroblastic anaemia
X pattern strabismus
X pattern vergence
X-linked Charcot-Marie-Tooth disease type 1
X-linked Charcot-Marie-Tooth disease type 2
X-linked Charcot-Marie-Tooth disease type 3
X-linked Charcot-Marie-Tooth disease type 4
X-linked Charcot-Marie-Tooth disease type 5
X-linked Charcot-Marie-Tooth disease type 6
X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome
X-linked absence of thyroxine-binding globulin
X-linked acrogigantism due to Xq26 microduplication
X-linked agammaglobulinaemia
X-linked agammaglobulinaemia with growth hormone deficiency
X-linked asexual dwarfism
X-linked calvarial hyperostosis
X-linked central congenital hypothyroidism with late-onset testicular enlargement
X-linked cerebral, cerebellar, coloboma syndrome
X-linked cleft palate and ankyloglossia
X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome
X-linked cone dysfunction syndrome with myopia
X-linked congenital dyserythropoietic anaemia with thrombocytopenia
X-linked corneal dermoid
X-linked creatine deficiency
X-linked diffuse leiomyomatosis with Alport syndrome
X-linked distal arthrogryposis multiplex congenita
X-linked distal spinal muscular atrophy type 3
X-linked dominant chondrodysplasia Chassaing Lacombe type
X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia
X-linked dyskeratosis congenita
X-linked dystonia parkinsonism
X-linked endothelial corneal dystrophy
X-linked epilepsy with learning disability and behaviour disorder syndrome
X-linked excess of thyroxine-binding globulin
X-linked hereditary disease
X-linked hereditary motor and sensory neuropathy
X-linked hereditary sensory and autonomic neuropathy with deafness
X-linked hereditary spastic paraplegia
X-linked hydrocephalus syndrome
X-linked hyper-IgM syndrome
Hypoparathyroidism - X-linked
X-linked ichthyosis with steryl-sulfatase deficiency
X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
X-linked immunoneurologic disorder
Partington syndrome
Christianson syndrome
X-linked intellectual disability Abidi type
X-linked intellectual disability Armfield type
Atkin Flaitz syndrome
X-linked intellectual disability Brooks type
X-linked intellectual disability Cabezas type
X-linked intellectual disability Cantagrel type
X-linked intellectual disability Cilliers type
X-linked intellectual disability Hedera type
X-linked intellectual disability Miles-Carpenter type
X-linked intellectual disability Nascimento type
X-linked intellectual disability Pai type
X-linked intellectual disability Schimke type
X-linked intellectual disability Seemanova type
X-linked intellectual disability Shrimpton type
X-linked intellectual disability Siderius type
X-linked intellectual disability Snyder type
X-linked intellectual disability Stevenson type
X-linked intellectual disability Stocco Dos Santos type
X-linked intellectual disability Stoll type
X-linked intellectual disability Turner type
X-linked intellectual disability Van Esch type
X-linked intellectual disability Wilson type
X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behaviour syndrome
X-linked intellectual disability due to GRIA3 mutations
X-linked intellectual disability with acromegaly and hyperactivity syndrome
X-linked intellectual disability with ataxia and apraxia syndrome
X-linked intellectual disability with cerebellar hypoplasia syndrome
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome
X-linked intellectual disability with hypogammaglobulinaemia and progressive neurological deterioration syndrome
X-linked intellectual disability with marfanoid habitus
X-linked intellectual disability with plagiocephaly syndrome
X-linked intellectual disability with seizure and psoriasis syndrome
X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome
X-linked intellectual disability, craniofacioskeletal syndrome
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome
X-linked intellectual disability, macrocephaly, macroorchidism syndrome
X-linked intellectual disability-psychosis-macroorchidism syndrome
X-linked lethal multiple pterygium syndrome
X-linked limb girdle muscular dystrophy with normal dystrophin
X-linked lissencephaly with abnormal genitalia syndrome
X-linked lymphoproliferative syndrome
X-linked mandibulofacial dysostosis
X-linked mendelian susceptibility to mycobacterial disease
X-linked muscular dystrophy not predominantly limb girdle
X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with limb girdle distribution
X-linked myopathy with excessive autophagy
X-linked myopathy with postural muscle atrophy
X-linked neurodegenerative syndrome Bertini type
X-linked neurodegenerative syndrome Hamel type

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