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SNOMED CT® Release Format 1 (RF1) Guide - ihtsdo

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236 | <strong>SNOMED</strong> CT <strong>Release</strong> <strong>Format</strong> 1 (<strong>RF1</strong>) <strong>Guide</strong> July 2012<br />

CONCEPTID<br />

53889007<br />

44248001<br />

95837007<br />

127062003<br />

64779008<br />

86075001<br />

128105004<br />

128115005<br />

61653009<br />

123976001<br />

19168005<br />

127326005<br />

127346000<br />

<strong>SNOMED</strong>ID<br />

DA-73540<br />

DA-78238<br />

DC-10190<br />

DC-38001<br />

DC-60000<br />

DC-63000<br />

DC-64101<br />

DC-64211<br />

DD-12432<br />

DE-00004<br />

DE-01200<br />

DF-000D3<br />

DF-000F9<br />

FULLY SPECIFIED NAME<br />

Nuclear cataract (disorder)<br />

Raymond-Cestan syndrome<br />

(disorder)<br />

Central cyanosis (disorder)<br />

Erythrocytosis (disorder)<br />

Blood coagulation disorder<br />

(disorder)<br />

Coagulation factor deficiency<br />

syndrome (disorder)<br />

Von Willebrand disorder<br />

(disorder)<br />

Pseudo von Willebrand<br />

disease (disorder)<br />

Bennett's fracture (disorder)<br />

Post-infectious disorder<br />

(disorder)<br />

Nosocomial infectious disease<br />

(disorder)<br />

Non-human disorder<br />

(disorder)<br />

Neurologic disorder of eye<br />

movements (disorder)<br />

DEFINITION<br />

A cataract involving the nucleus of the lens<br />

Abducent nerve paralysis with contralateral<br />

hemiparesis<br />

A form of cyanosis that occurs when there is<br />

a decrease in oxygen saturation in the arterial<br />

blood, usually with an SaO2 of below 75%<br />

Peripheral blood red cell count above the<br />

normal range<br />

Disorders involving the elements of blood<br />

coagulation, including platelets, coagulation<br />

factors and inhibitors, and the fibrinolytic<br />

system<br />

Includes both quantitative and qualitative<br />

disorders of procoagulants<br />

Includes true von Willebrand disease with<br />

mutation at the VWF locus, as well as<br />

mimicking disorders with other mutations<br />

(pseudo VWD) and acquired von Willebrand<br />

syndrome<br />

Any inherited disorder mimicking von<br />

Willebrand disease but lacking mutation at<br />

the VWF locus<br />

Fracture and dislocation of the first metacarpal<br />

and the carpal-metacarpal joint<br />

A disorder that follows infection but is distinct<br />

from the infection itself and its usual<br />

manifestations<br />

Infection associated with hospitalization , not<br />

present or incubating prior to admission, but<br />

generally occurring more than 72 hours after<br />

admission<br />

Disorders which occur in animals but not in<br />

man<br />

Disorders characterized by eye movement<br />

abnormalities that are the result of brain,<br />

cranial nerve, or neuromuscular junction<br />

dysfunction<br />

© 2002-2012 International Health Terminology Standards Development Organisation CVR #: 30363434

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