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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
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
Autosomal recessive hyperinsulinism due to SUR1 deficiency
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
Autosomal recessive hypophosphataemic bone disease
Autosomal recessive hypophosphataemic rickets
Autosomal recessive hypophosphataemic vitamin D refractory rickets
Autosomal recessive ichthyosis
Autosomal recessive idiopathic familial dystonia
Autosomal recessive infantile hypercalcaemia
Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
Autosomal recessive isolated somatotropin deficiency
Autosomal recessive keratitis-ichthyosis-deafness syndrome
Autosomal recessive leukoencephalopathy, ischaemic stroke, retinitis pigmentosa syndrome
Autosomal recessive limb girdle muscular dystrophy type 2A
Autosomal recessive limb girdle muscular dystrophy type 2B
Autosomal recessive limb girdle muscular dystrophy type 2C
Autosomal recessive limb girdle muscular dystrophy type 2D
Autosomal recessive limb girdle muscular dystrophy type 2E
Autosomal recessive limb girdle muscular dystrophy type 2F
Autosomal recessive limb girdle muscular dystrophy type 2G
Autosomal recessive limb girdle muscular dystrophy type 2I
Autosomal recessive limb girdle muscular dystrophy type 2J
Autosomal recessive limb girdle muscular dystrophy type 2K
Autosomal recessive limb girdle muscular dystrophy type 2L
Autosomal recessive limb girdle muscular dystrophy type 2M
Autosomal recessive limb girdle muscular dystrophy type 2N
Autosomal recessive limb girdle muscular dystrophy type 2O
Autosomal recessive limb girdle muscular dystrophy type 2P
Autosomal recessive limb girdle muscular dystrophy type 2Q
Autosomal recessive limb girdle muscular dystrophy type 2S
Autosomal recessive limb girdle muscular dystrophy type 2T
Autosomal recessive limb girdle muscular dystrophy type 2U
Autosomal recessive limb girdle muscular dystrophy type 2Y
Autosomal recessive lower motor neuron disease with childhood onset
Autosomal recessive lymphoproliferative disease
Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
Autosomal recessive muscular dystrophy not predominantly limb girdle
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
Autosomal recessive muscular dystrophy with limb girdle distribution
Autosomal recessive myogenic arthrogryposis multiplex congenita
Autosomal recessive nail dysplasia
Autosomal recessive ocular albinism
Autosomal recessive omodysplasia
Autosomal recessive optic atrophy type 6
Autosomal recessive optic atrophy OPA7 type
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome
Bartsocas Papas syndrome
Posterior column ataxia with retinitis pigmentosa syndrome
Autosomal recessive primary microcephaly
Autosomal recessive progressive external ophthalmoplegia
Autosomal recessive pseudoxanthoma elasticum
Autosomal recessive retinitis pigmentosa
Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
Autosomal recessive SCID (severe combined immunodeficiency disease)
Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
Autosomal recessive sideroblastic anaemia
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Autosomal recessive spastic ataxia with leukoencephalopathy
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
Autosomal recessive spastic paraplegia type 11
Autosomal recessive spastic paraplegia type 14
Autosomal recessive spastic paraplegia type 15
Autosomal recessive spastic paraplegia type 18
Autosomal recessive spastic paraplegia type 21
Autosomal recessive spastic paraplegia type 23
Autosomal recessive spastic paraplegia type 24
Autosomal recessive spastic paraplegia type 25
Autosomal recessive spastic paraplegia type 26
Autosomal recessive spastic paraplegia type 27
Autosomal recessive spastic paraplegia type 28
Autosomal recessive spastic paraplegia type 32
Autosomal recessive spastic paraplegia type 35
Autosomal recessive spastic paraplegia type 39
Autosomal recessive spastic paraplegia type 43
Autosomal recessive spastic paraplegia type 44
Autosomal recessive spastic paraplegia type 45
Autosomal recessive spastic paraplegia type 46
Autosomal recessive spastic paraplegia type 48
Autosomal recessive spastic paraplegia type 53
Autosomal recessive spastic paraplegia type 54
Autosomal recessive spastic paraplegia type 55
Autosomal recessive spastic paraplegia type 56
Autosomal recessive spastic paraplegia type 57
Autosomal recessive spastic paraplegia type 58
Autosomal recessive spastic paraplegia type 59
Autosomal recessive spastic paraplegia type 5A
Autosomal recessive spastic paraplegia type 60
Autosomal recessive spastic paraplegia type 61
Autosomal recessive spastic paraplegia type 62
Autosomal recessive spastic paraplegia type 63
Autosomal recessive spastic paraplegia type 64
Autosomal recessive spastic paraplegia type 66
Autosomal recessive spastic paraplegia type 67
Autosomal recessive spastic paraplegia type 69

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