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

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

CONCEPTID<br />

413577001<br />

95442007<br />

128065004<br />

111029001<br />

111030006<br />

109478007<br />

128533009<br />

93040009<br />

94684003<br />

75076004<br />

109750005<br />

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

D3-80064<br />

D3-80506<br />

D4-38016<br />

D4-40131<br />

D4-40139<br />

D4-51098<br />

D4-A0655<br />

D4-A0806<br />

D4-A0824<br />

D4-F1137<br />

D5-15106<br />

FULLY SPECIFIED NAME<br />

Arterial thoracic outlet<br />

syndrome due to cervical rib<br />

(disorder)<br />

Peripheral cyanosis (disorder)<br />

Congenital partial<br />

portal-systemic shunt<br />

(disorder)<br />

Acrokerato-elastoidosis<br />

(disorder)<br />

Howel-Evans' syndrome<br />

(disorder)<br />

Kohlschutter's syndrome<br />

(disorder)<br />

Micropapilla (disorder)<br />

Congenital blepharophimosis<br />

(disorder)<br />

Microblepharia (disorder)<br />

Amyelencephalus (disorder)<br />

Abfraction (disorder)<br />

DEFINITION<br />

Thoracic outlet syndrome, either nerve or<br />

vessel compression, due to a cervical rib<br />

Disorder characterized by slowing of blood<br />

flow to a body region in association with an<br />

increase in oxygen extraction from normally<br />

saturated arterial blood<br />

Congenital portal-systemic shunt in which at<br />

least some portal blood perfuses the liver<br />

A developmental disorder characterized by<br />

keratotic papules of skin of hands and soles<br />

with disorganization of dermal elastic fibers<br />

that does not appear to be due to trauma or<br />

sunlight<br />

A form of diffuse palmoplantar keratoderma<br />

that occurs between the ages of 5 and 15 and<br />

may be associated with the subsequent<br />

development of esophageal cancer<br />

Ameliogenesis imperfecta, mental retardation,<br />

and epileptic seizures<br />

Congenital small optic disc with normal visual<br />

function<br />

A decrease in size of opening of the eye, not<br />

due to eyelid fusion, but rather lateral<br />

displacement of the inner canthi<br />

Congenital abnormal vertical shortness of<br />

eyelids<br />

Congenital absence of the spinal cord and<br />

brain<br />

Noncarious lesion, where tooth is fatigued,<br />

flexed, and deformed by biomechanical<br />

loading of the tooth structure, primarily at the<br />

cervical region. These are usually<br />

wedge-shaped lesions with sharp-line angles,<br />

but sometimes are circular invaginations on<br />

occlusal surfaces.<br />

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

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