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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
X-linked intellectual disability Cabezas type
X-linked intellectual disability Cantagrel type
X-linked intellectual disability Cilliers type
X-linked intellectual disability Hedera type
X-linked intellectual disability Miles-Carpenter type
X-linked intellectual disability Nascimento type
X-linked intellectual disability Pai type
X-linked intellectual disability Schimke type
X-linked intellectual disability Seemanova type
X-linked intellectual disability Shrimpton type
X-linked intellectual disability Siderius type
X-linked intellectual disability Snyder type
X-linked intellectual disability Stevenson type
X-linked intellectual disability Stocco Dos Santos type
X-linked intellectual disability Stoll type
X-linked intellectual disability Turner type
X-linked intellectual disability Van Esch type
X-linked intellectual disability Wilson type
X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behaviour syndrome
X-linked intellectual disability due to GRIA3 mutations
X-linked intellectual disability hypotonic face syndrome
X-linked intellectual disability with acromegaly and hyperactivity syndrome
X-linked intellectual disability with ataxia and apraxia syndrome
X-linked intellectual disability with cerebellar hypoplasia syndrome
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome
X-linked intellectual disability with hypogammaglobulinaemia and progressive neurological deterioration syndrome
X-linked intellectual disability with marfanoid habitus
X-linked intellectual disability with plagiocephaly syndrome
X-linked intellectual disability with seizure and psoriasis syndrome
X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome
X-linked intellectual disability, craniofacioskeletal syndrome
X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
X-linked intellectual disability, hypotonia, movement disorder syndrome
X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome
X-linked intellectual disability, macrocephaly, macroorchidism syndrome
X-linked intellectual disability, short stature, overweight syndrome
X-linked intellectual disability-psychosis-macroorchidism syndrome
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome
X-linked lethal multiple pterygium syndrome
X-linked limb girdle muscular dystrophy with normal dystrophin
X-linked lissencephaly with abnormal genitalia syndrome
X-linked lymphoproliferative disease due to SH2D1A deficiency
X-linked lymphoproliferative disease due to XIAP deficiency
X-linked lymphoproliferative syndrome
X-linked mandibulofacial dysostosis
X-linked mendelian susceptibility to mycobacterial disease
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome
X-linked muscular dystrophy not predominantly limb girdle
X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with limb girdle distribution
X-linked myopathy with excessive autophagy
X-linked myopathy with postural muscle atrophy
X-linked myotubular myopathy, abnormal genitalia syndrome
X-linked neurodegenerative syndrome Bertini type
X-linked neurodegenerative syndrome Hamel type
X-linked non progressive cerebellar ataxia
X-linked oligodontia
X-linked optic atrophy
X-linked osteoporosis with fractures
Panhypopituitarism - X-linked
X-linked parkinsonism with spasticity syndrome
X-linked periventricular heterotopia
X-linked progressive cerebellar ataxia
X-linked pure hereditary spastic paraplegia
X-linked recessive hereditary disease
X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome
X-linked recessive nephrolithiasis with renal failure
X-linked recessive sensory neuropathy
X-linked reduction of thyroxine-binding globulin
X-linked reticulate pigmentary disorder with systemic manifestation syndrome
X-linked retinal dysplasia
X-linked retinitis pigmentosa
X-linked retinitis pigmentosa heterozygote
X-linked scapuloperoneal muscular dystrophy
X-linked sensorineural hearing loss
X-linked severe congenital neutropenia
X-linked sideroblastic anaemia with spinocerebellar ataxia
X-linked spastic paraplegia type 16
Spastic paraplegia type 2
X-linked spastic paraplegia type 34
X-linked spasticity, intellectual disability, epilepsy syndrome
X-linked spinocerebellar ataxia type 3
X-linked spinocerebellar ataxia type 4
X-linked spondyloepimetaphyseal dysplasia
X-linked thrombocytopaenia with normal platelets
X-linked variant form of thyroxine-binding globulin
X-ray contrast media adverse reaction
X-ray contrast media overdose
X-ray contrast media poisoning
X-ray evidence of poor mineralization
X-ray of fibula abnormal
X-ray of fibula normal
X-ray of gastrointestinal tract abnormal
X-ray of genitourinary system abnormal
X-ray of head abnormal
X-ray of musculoskeletal system abnormal
X-ray of thumb abnormal

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