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32570061000036105: Body structure 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
108642071000036111 Body structure foundation reference set (foundation metadata concept) en Fully specified name Active Case insensitive SNOMED Clinical Terms Australian extension
108642081000036113 Body structure foundation reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension
4350821000168112 <p>Supports the recording of anatomical structures in Australian e-health implementations.</p><p>This reference set can be used:<ul><li>Within implementations where use-case specific reference sets for body structure are yet to be developed.</li><li>As the basis for developing further use-case specific reference sets for body structure, through a process of constraint.</li><li>As a benchmark, against which use-case specific reference sets developed by the SNOMED CT-AU user community can be tested to assure that they are logical constraints of the body structure content.</li></ul></p><p><b>Target client: </b>NCTS</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


40912 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Body structure foundation reference set Developed by Australian Digital Health Agency true Inferred relationship Some 845697486
Body structure foundation reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 96736961
Body structure foundation reference set Is a Foundation reference sets true Inferred relationship Some
Body structure foundation reference set Is a Attribute value type false Inferred relationship Some
Body structure foundation reference set Is a Simple type reference set true Inferred relationship Some

Members
Acquired body structure
Acquired dysplasia
Acquired fistula
Acquired heterotopic structure
Acquired stenosis
Acquired web
Acral lentiginous melanoma, malignant
Acral naevus
Acromioclavicular joint structure
Acrosomal granule
Acrosomal vesicle
Actinic keratosis
Actinotherapy effect
Active caries
Active cavitated caries
Active congestion
Active non-cavitated caries
Acupuncture point
Acute abscess
Acute and chronic inflammation
Acute atrophy
Acute basophilic leukaemia
Acute biphenotypic leukaemia
Acute bleeding ulcer
Acute cellulitis
Acute collapse
Acute congestion
Acute dilatation
Acute oedema
Acute emphysema
Acute emphysematous inflammation
Acute empyema
Acute eosinophilic leukaemia
Acute exudative inflammation
Acute fibrinopurulent inflammation
Acute fibrinous inflammation
Acute fibrosis
Acute haemorrhage
Acute haemorrhagic inflammation
Acute hydrops
Acute hypertrophy
Acute infarct
Acute inflammation
Acute inflammatory morphology
Acute leukaemia
Acute leukaemia of ambiguous lineage
Acute lymphoid follicular inflammation
Acute lysis
Acute megakaryoblastic leukaemia
Acute membranous inflammation
Acute monoblastic and monocytic leukaemia
Acute monocytic leukaemia
Acute mucous inflammation
Acute multifocal inflammation
Acute myeloid leukaemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1
Acute myeloid leukaemia
Acute myeloid leukaemia with BCR-ABL1
Acute myeloid leukaemia with FMS-like tyrosine kinase-3 mutation
Acute myeloid leukaemia with abnormal marrow eosinophils
Acute myeloid leukaemia with biallelic mutation of CEBPA (CCAAT enhancer binding protein alpha) gene
Acute myeloid leukaemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1
Acute myeloid leukaemia with maturation
Acute myeloid leukaemia with multilineage dysplasia
Acute myeloid leukaemia with multilineage dysplasia following a myelodysplastic syndrome or myelodysplastic syndrome/myeloproliferative disorder
Acute myeloid leukaemia with multilineage dysplasia without antecedent myelodysplastic syndrome
Acute myeloid leukaemia with mutated NPM1
Acute myeloid leukaemia with mutated RUNX1
Acute myeloid leukaemia with mutation of CEBPA (CCAAT enhancer binding protein alpha) gene
Acute myeloid leukaemia with recurrent genetic abnormality
Acute myeloid leukaemia with t(6;9)(p23;q34); DEK-NUP214
Acute myeloid leukaemia with t(8;16)(p11;p13) translocation
Acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL
Acute myeloid leukaemia without maturation
Acute myeloid leukaemia, 11q23 abnormalities
Acute myeloid leukaemia, M6 type
Acute myeloid leukaemia, minimal differentiation
Acute myeloid leukaemia, t(8;21) (q22;q22)
Acute myelomonocytic leukaemia
Acute necrosis
Acute necrotising inflammation
Acute obstruction
Acute panmyelosis with myelofibrosis
Acute passive congestion
Acute proliferative inflammation
Acute promyelocytic leukaemia
Acute pseudomembranous inflammation
Acute radiation injury
Acute radiation ulcer
Acute serofibrinous inflammation
Acute serous inflammation
Acute superficial ulcer
Acute suppurative inflammation
Acute ulcer
Acute ulcerative inflammation
Acute vesicular inflammation
Adamantinoma of long bones
Adduction contracture
Adduction deformity
Adductor hallucis muscle structure
Adductor longus muscle structure
Adductor pollicis muscle structure

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