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112641009: Telangiectasis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
183290017 Telangiectasis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
190374016 Telangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
642136019 Telangiectasis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
830091000241117 télangiectasie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Telangiectasis Is a Mechanical abnormality false Inferred relationship Some
Telangiectasis Is a Mechanical lesion true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Venous telangiectases of the lower limb Associated morphology False Telangiectasis Inferred relationship Some 3
TEMPI syndrome is a rare multi-systemic disease characterized by the presence of Telangiectasias, Erythrocytosis with elevated erythropoietin levels, Monoclonal gammopathy, Perinephric-fluid collections, and Intrapulmonary shunting. Associated morphology True Telangiectasis Inferred relationship Some 7
An extremely rare syndromic lymphedema disorder characterized by early-onset hypotrichosis, childhood-onset lymphedema, and variable telangiectasia, particularly of the palms. Associated morphology False Telangiectasis Inferred relationship Some 5
A rare, genetic, epilepsy syndrome characterized by epilepsy, palpebral conjunctival telangiectasias, borderline to moderate intellectual disability, diminished serum IgA levels, shortened fifth fingers and dysmorphic facial features (including frontal hirsutism, synophrys, anteverted nostrils, prominent ears, long philtrum, irregular teeth implantation, micrognathia). No new cases have been described in the literature since 1978. Associated morphology False Telangiectasis Inferred relationship Some 8
Telangiectasia of macula lutea Associated morphology True Telangiectasis Inferred relationship Some 2
Telangiectasia of macula lutea Associated morphology True Telangiectasis Inferred relationship Some 3
Unilateral nevoid telangiectasia Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of left retina (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of right retina Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of bilateral retinas (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of bilateral retinas (disorder) Associated morphology True Telangiectasis Inferred relationship Some 2
A rare, genetic, epilepsy syndrome characterized by epilepsy, palpebral conjunctival telangiectasias, borderline to moderate intellectual disability, diminished serum IgA levels, shortened fifth fingers and dysmorphic facial features (including frontal hirsutism, synophrys, anteverted nostrils, prominent ears, long philtrum, irregular teeth implantation, micrognathia). No new cases have been described in the literature since 1978. Associated morphology True Telangiectasis Inferred relationship Some 3
Idiopathic macular telangiectasia type 1 is a rare, acquired, eye disease characterized by unilateral (rarely bilateral) abnormally dilated and tortuous capillaries around the fovea, associated with multiple arteriolar and venular aneurysms, lipid depositions, and intra-retinal cystoid degeneration. It leads to vision loss due to macular edema with hard exudates. Associated morphology True Telangiectasis Inferred relationship Some 2
Idiopathic macular telangiectasia type 1 is a rare, acquired, eye disease characterized by unilateral (rarely bilateral) abnormally dilated and tortuous capillaries around the fovea, associated with multiple arteriolar and venular aneurysms, lipid depositions, and intra-retinal cystoid degeneration. It leads to vision loss due to macular edema with hard exudates. Associated morphology True Telangiectasis Inferred relationship Some 1
Idiopathic macular telangiectasia type 3 is a rare, acquired, eye disease characterized by progressive visual loss, due to bilateral juxtafoveolar capillary occlusions, capillary telangiectasia, and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease. Associated morphology True Telangiectasis Inferred relationship Some 1
Idiopathic macular telangiectasia type 3 is a rare, acquired, eye disease characterized by progressive visual loss, due to bilateral juxtafoveolar capillary occlusions, capillary telangiectasia, and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease. Associated morphology True Telangiectasis Inferred relationship Some 2
Spider veins of bilateral lower limbs (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Spider veins of bilateral lower limbs (disorder) Associated morphology True Telangiectasis Inferred relationship Some 2
Spider veins of bilateral lower limbs (disorder) Associated morphology False Telangiectasis Inferred relationship Some 3
A rare, inherited cancer-predisposing syndrome characterized by an early development of cutaneous telangiectasia, mild dental and nail anomalies, patchy alopecia over the affected skin areas and increased lifetime risk for oropharyngeal cancer. Other types of cancer have also been reported. Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of limb Associated morphology True Telangiectasis Inferred relationship Some 1
Venous telangiectases of the lower limb Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of skin of face Associated morphology True Telangiectasis Inferred relationship Some 1
Idiopathic macular telangiectasia type 2 (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Idiopathic macular telangiectasia type 2 (disorder) Associated morphology True Telangiectasis Inferred relationship Some 2
Idiopathic juxtafoveal telangiectasia (disorder) Associated morphology True Telangiectasis Inferred relationship Some 2
Acquired telangiectasia of small and large intestines Associated morphology True Telangiectasis Inferred relationship Some 2
Acquired telangiectasia of small and large intestines Associated morphology True Telangiectasis Inferred relationship Some 1
An extremely rare syndromic lymphedema disorder characterized by early-onset hypotrichosis, childhood-onset lymphedema, and variable telangiectasia, particularly of the palms. Associated morphology True Telangiectasis Inferred relationship Some 2
Syndrome with characteristics of co-occurrence of both juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia. Juvenile polyposis syndrome has characteristics of hamartomatous polyps occurring throughout the gastrointestinal tract. Hereditary hemorrhagic telangiectasia is characterized by vascular dysplasia with telangiectases of the skin, oral and nasal mucosa and arteriovenous malformation of the lungs, liver, brain and gastrointestinal tract. The syndrome is caused by heterozygous mutation in the SMAD4 gene on chromosome 18q21. Associated morphology True Telangiectasis Inferred relationship Some 1
Acquired peripheral retinal telangiectasia (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Hereditary hemorrhagic telangiectasia of gingiva Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of skin (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Spider telangiectasis of skin Associated morphology True Telangiectasis Inferred relationship Some 1
Drug-induced telangiectasia Associated morphology True Telangiectasis Inferred relationship Some 1
Photodistributed telangiectasia (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Rosacea, erythematous telangiectatic type (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Microsclerotherapy to spider veins of leg Direct morphology True Telangiectasis Inferred relationship Some 1
Necrobiosis lipoidica, granulomatous type Associated morphology True Telangiectasis Inferred relationship Some 4
Necrobiosis lipoidica diabeticorum Associated morphology True Telangiectasis Inferred relationship Some 4
Granulomatosis disciformis et progressiva Associated morphology True Telangiectasis Inferred relationship Some 5
Necrobiosis lipoidica, necrobiotic type Associated morphology True Telangiectasis Inferred relationship Some 4
Necrobiosis lipoidica Associated morphology True Telangiectasis Inferred relationship Some 4
Telangiectasia of colon Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasis of vocal fold Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasis of vocal cord following radiotherapy Associated morphology True Telangiectasis Inferred relationship Some 2
Telangiectasia of macula lutea of left eye (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of macula lutea of left eye (disorder) Associated morphology True Telangiectasis Inferred relationship Some 2
Telangiectasia of macula lutea of right eye (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of macula lutea of right eye (disorder) Associated morphology True Telangiectasis Inferred relationship Some 2
Telangiectasia of macula lutea of bilateral eyes (disorder) Associated morphology True Telangiectasis Inferred relationship Some 1
Telangiectasia of macula lutea of bilateral eyes (disorder) Associated morphology True Telangiectasis Inferred relationship Some 2
Telangiectasia of macula lutea of bilateral eyes (disorder) Associated morphology True Telangiectasis Inferred relationship Some 3
Telangiectasia of macula lutea of bilateral eyes (disorder) Associated morphology True Telangiectasis Inferred relationship Some 4

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