32570581000036105: Problem/Diagnosis reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept\Reference set\...

\Australian reference sets\Reference set by clinical information component\Reference sets for Problem/diagnosis\Problem/Diagnosis reference set

\Simple type reference set\Problem/Diagnosis reference set

Status: current, Primitive. Date: 31-May 2012. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module

108644681000036112 Problem/Diagnosis reference set (foundation metadata concept) en Fully specified name Active Initial character case insensitive SNOMED Clinical Terms Australian extension

108644691000036114 Problem/Diagnosis reference set en Synonym Active Initial character case insensitive SNOMED Clinical Terms Australian extension

4351251000168110 <p>Supports the recording of a patient problem or diagnosis for medical records within Australia.</p><p>This reference set can be used within implementations of the <em>Medical History DCM</em> (<em>Medical History Detailed Clinical Model Specification.</em> Sydney: NEHTA; 2015. v1.0.).</p><p><b>Target client: </b>This reference set has been developed for those who are implementing the <em>Medical History DCM.</em></p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Problem/Diagnosis reference set	Has licence	SNOMED CT-AU licence	true	Inferred relationship	Some	1629158626
Problem/Diagnosis reference set	Developed by	Australian Digital Health Agency	true	Inferred relationship	Some	880198101
Problem/Diagnosis reference set	Is a	Reference sets for Problem/diagnosis	true	Inferred relationship	Some
Problem/Diagnosis reference set	Is a	Attribute value type	false	Inferred relationship	Some
Problem/Diagnosis reference set	Is a	Simple type reference set	true	Inferred relationship	Some

Members

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 exposure accident

X-ray metastasis control

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

X-ray of thumb normal

X-ray of tibia abnormal

X-ray of tibia normal

X-ray of tibia/fibula abnormal

X-ray of tibia/fibula normal

X-ray pelvimetry abnormal

X-ray pelvimetry normal

X-ray phalanges of fingers abnormal

X-ray phalanges of fingers normal

X-ray radiotherapy control

X-ray shoulder/arm abnormal

X-ray shoulder/arm normal

X-ray thoracic cage abnormal

X-ray thoracic cage normal

XK aprosencephaly syndrome

XY type gonadal dysgenesis with associated anomalies syndrome

XY, female phenotype

X^o^rX^o^r blood group phenotype

Xamoterol adverse reaction

Increased xanthine

Xanthine adverse reaction

Xanthine and/or xanthine derivative overdose

Decreased xanthine

Xanthine overdose

Xanthine oxidase inhibitor adverse reaction

Xanthine within reference range

Xanthium species poisoning

Xanthogranuloma

Xanthogranuloma of choroid plexus

Xanthogranulomatous cholecystitis

Xanthomatous hypophysitis

Xanthogranulomatous pyelonephritis

Xanthogranulomatous salpingitis

Xanthoma diabeticorum

Xanthoma disseminatum

Xanthoma due to abnormality of lipid metabolism

Xanthoma due to lipid storage disease

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