FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.4  |  FHIR Version n/a  User: [n/a]

32570071000036102: Clinical finding foundation reference set (foundation metadata concept)


Status: current, Primitive. Date: 30-Nov 2009. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module
108642091000036110 Clinical finding foundation reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension
108642101000036118 Clinical finding foundation reference set (foundation metadata concept) en Fully specified name Active Case insensitive SNOMED Clinical Terms Australian extension
4350871000168113 <p>Supports the recording of clinical findings and disorders in Australian e-health implementations.</p><p>This reference set can be used:<ul><li>Within implementations where use-case specific reference sets for clinical findings and disorders are yet to be developed.</li><li>As the basis for developing further use-case specific reference sets for clinical findings and disorders, through a process of constraint.</li><li>As a benchmark against which use-case specific reference sets that have been developed by the SNOMED CT-AU user community can be tested to assure that they are logical constraints of content related to clinical finding and disorders.</li></ul></p><p><b>Target client: </b>NCTS</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


115151 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Clinical finding foundation reference set Developed by Australian Digital Health Agency true Inferred relationship Some 1641902964
Clinical finding foundation reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1904103807
Clinical finding foundation reference set Is a Foundation reference sets true Inferred relationship Some
Clinical finding foundation reference set Is a Attribute value type false Inferred relationship Some
Clinical finding foundation reference set Is a Simple type reference set true Inferred relationship Some

Members
Wrinkled skin
Wrinkly skin syndrome
Wrist clonus
Left wrist drop
Right wrist drop
Wrist impingement syndrome
Wrist joint - cold
Wrist joint - cool
Wrist joint - hot
Wrist joint - soft tissue swelling
Wrist joint - synovial swelling
Wrist joint - warm
Wrist joint crepitus
Wrist joint crepitus audible
Wrist joint crepitus palpable
Wrist joint deformity
Wrist joint effusion
Wrist joint hypermobility
Wrist joint inflamed
Wrist joint laxity
Wrist joint pain
Wrist joint painful on movement
Wrist joint prosthesis present
Wrist joint red
Wrist joint stable
Wrist joint unstable
Wrist pyogenic arthritis
Wrist sign
Stiffness of wrist
Wrist symptom
Wristdrop
Writer's cramp neurosis
Writhing movements
Writing epilepsy
Wrong power intraocular lens
Wrong tissue received
Wyeomyia virus disease
X chromosome-linked pyridoxine refractory sideroblastic anaemia
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 Emery-Dreifuss muscular dystrophy
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 complex hereditary spastic paraplegia
X-linked complicated corpus callosum dysgenesis
X-linked cone dysfunction syndrome with myopia
X-linked congenital dyserythropoietic anaemia with thrombocytopenia
X-linked congenital generalised hypertrichosis
X-linked corneal dermoid
X-linked creatine deficiency
X-linked diffuse leiomyomatosis with Alport syndrome
X-linked distal arthrogryposis multiplex congenita
X-linked distal hereditary motor neuropathy
X-linked distal spinal muscular atrophy type 3
X-linked dominant chondrodysplasia Chassaing Lacombe type
X-linked dominant erythropoietic protoporphyria
X-linked dominant hereditary disease
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 external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome
X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability
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
X-linked hypodontia
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

Start Previous Page 1148 of 1152 Next End


Reference Sets

Reference set descriptor

Back to Start