FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.9.0  |  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
Adrenocortical haemorrhage
Adrenocortical hyperfunction
Adrenocortical hyperplasia
Adrenocortical hypofunction following procedure
ACTH deficiency
ACTH hypersecretion
ACTH hypersecretion not causing Cushing's syndrome
Increased adrenocorticotropic hormone level
Decreased adrenocorticotropic hormone level
Adrenocorticotropic hormone resistance syndrome
Adrenocorticotropic hormone within reference range
ACTH-dependent Cushing's syndrome
Adrenogenital disorder
Drug-induced adrenogenital disorder
Adrenoleucodystrophy
Adrenomedullary hyperplasia
Adrenomyodystrophy
Adson's sign
Adult Fanconi syndrome
Adult GM1 gangliosidosis
Adult T-cell leukaemia/lymphoma
Adult T-cell leukaemia/lymphoma in remission
Adult T-cell leukaemia/lymphoma of skin
Adult acute epiglottitis and supraglottitis
Adult antisocial behaviour
Adult atopic dermatitis
Adult atopic dermatitis commencing in adult life
Adult atopic dermatitis persistent from childhood
Adult atopic dermatitis recurrent in adult life
Adult atopic flexural dermatitis
Adult attention deficit hyperactivity disorder
Adult behaviour alteration
Adult bronchiectasis
Adult chronic GM2 gangliosidosis
Adult chronic idiopathic neutropenia
Adult chronic lichenified atopic dermatitis
Adult colic
Adult degenerative scoliosis deformity of spine
Adult diabetes diet
Adult disease
Adult dyssocial behaviour
Adult education
Adult failure to thrive syndrome
Adult familial nephronophthisis with spastic quadriparesia syndrome
Adult form of coeliac disease
Adult foster home living
Adult fucosidosis
Adult gender identity disorder, sexually attracted to both sexes
Adult gender identity disorder, sexually attracted to females
Adult gender identity disorder, sexually attracted to males
Adult gender identity disorder, sexually attracted to neither sex
Adult generalised atopic dermatitis
Adult G6PD deficiency of leucocytes syndrome
Adult growth hormone deficiency
Adult growth hormone deficiency with onset in childhood
Adult habitual masturbation
Adult cardiac tumour
Adult hepatocellular carcinoma
Adult hydrocele
Adult hypertrophic pyloric stenosis
Adult hypophosphatasia
Adult idiopathic generalised osteoporosis
Adult immunisation - call deleted
Adult immunisation - recall deleted
Adult impetiginised atopic dermatitis
Adult intestinal botulism
Adult lichen sclerosus
Adult linear IgA disease
Adult myxoedema
Adult necrotising enterocolitis
Adult neuronal ceroid lipofuscinosis
Adult nummular atopic dermatitis
Adult onset Still's disease
Adult onset autosomal dominant leucodystrophy
Adult onset autosomal recessive muscular dystrophy with normal dystrophin
Adult onset dermatomyositis
Adult onset fluency disorder
Adult onset non-insulinoma persistent hyperinsulinaemic hypoglycaemia
Adult onset stuttering
Adult osteochondritis of spine
Adult osteochondrosis of cervical spine
Adult osteochondrosis of spine
Adult osteochondrosis of thoracic spine
Adult osteochondrosis of thoracolumbar spine
Adult osteomalacia due to endocrine disease
Adult osteomalacia due to liver disease
Adult osteomalacia due to malabsorption
Adult osteomalacia due to malnutrition
Adult pityriasis rubra pilaris
Adult polyglucosan body disease
Adult premenstrual acne
Adult pruriginous atopic dermatitis
Adult pubic hair in type and quantity with spread to medial surface of thigh
Adult pulmonary Langerhans cell histiocytosis
Adult pure red cell aplasia
Adult retinoschisis
Adult rhabdomyoma
Adult rumination syndrome of ingested food
Adult safeguarding concern
Adult screening - call deleted
Adult screening - recall deleted

Start Previous Page 71 of 1152 Next End


Reference Sets

Reference set descriptor

Back to Start