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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
Apgar at 10 minutes = 9
Apgar at 5 minutes = 0
Apgar at 5 minutes = 1
Apgar at 5 minutes = 10
Apgar at 5 minutes = 2
Apgar at 5 minutes = 3
Apgar at 5 minutes = 4
Apgar at 5 minutes = 5
Apgar at 5 minutes = 6
Apgar at 5 minutes = 7
Apgar at 5 minutes = 8
Apgar at 5 minutes = 9
Apgar normal
Apgar score 0
Apgar score 1
Apgar score 10
Apgar score 2
Apgar score 3
Apgar score 4
Apgar score 5
Apgar score 6
Apgar score 7
Apgar score 8
Apgar score 9
Aphagia
Aphagia algera
Aphakia
Aphakia - Elschnig's pearls
Aphakia - lens capsule present
Aphakia - no lens capsule
Traumatic aphakia
Bilateral eye aphakia
Aphakia of left eye
Aphakia of right eye
Aphakic bullous keratopathy of left eye
Aphakic bullous keratopathy of right eye
Aphakic corneal oedema
Aphalangy and syndactyly with microcephaly syndrome
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
Aphasia
Aphasia as late effect of stroke
Aphasia as late effect of cerebrovascular disease
Aphasia due to and following embolic cerebrovascular accident
Aphasia due to and following haemorrhagic stroke
Aphasia due to and following ischaemic stroke
Aphasia due to and following non-traumatic intracerebral haemorrhage
Aphasia due to and following non-traumatic subarachnoid haemorrhage
Aphasia due to brain damage
Aphasia, agnosia, dyslexia AND/OR apraxia
Aphasia-angular gyrus syndrome
Aphasia-left parietal lobe syndrome
Aphonia
Aphonia paralytica
Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome
Aphthae major
Aphthosis of glans penis
Aphthous ulcer of male genital organ
Aphthous ulcer of mouth
Aphthous ulceration of large intestine
Aphthous ulceration of skin and/or mucous membrane
Apical axillary lymphadenopathy
Apical callus
Apical diastolic thrill
Apical granuloma
Apical periodontitis
Aplasia cutis congenita
Aplasia cutis congenita associated with fetus papyraceus (Type 5)
Aplasia cutis congenita due to teratogenic drug (Type 7)
Aplasia cutis congenita due to underlying malformation (Type 4)
Aplasia cutis congenita following intra-uterine infection (Type 8)
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6)
Aplasia cutis congenita of limb
Aplasia cutis congenita secondary to malformation syndrome (Type 9)
Toriello Lacassie Droste syndrome
Aplasia cutis congenita with intestinal lymphangiectasia syndrome
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
Aplasia cutis in Johanson-Blizzard syndrome
Aplasia cutis in Trisomy 13 syndrome
Aplasia cutis with myopia syndrome
Aplasia of adrenal gland
Congenital aplasia of aorta
Aplasia of auditory canal
Aplasia of body of uterus
Aplasia of cementum
Aplasia of cerebellum
Aplasia of corpus callosum
Aplasia of diaphragm
Fibular aplasia and ectrodactyly syndrome
Fibular aplasia and complex brachydactyly
Aplasia of gallbladder
Aplasia of muscle
Aplasia of optic nerve
Aplasia of parathyroid gland
Aplasia of patella
Aplasia of penis
Aplasia of skin
Aplasia of spermatic cord
Aplasia of spleen
Aplasia of testicle
Aplasia of the cochlea and vestibular labyrinth
Aplasia of the vermis

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