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234095009: Lymphatic malformation (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
350729015 Lymphatic malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622370017 Lymphatic malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4992121000241113 malformation lymphatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

30 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lymphatic malformation Is a Disorder of lymphatic vessel (disorder) true Inferred relationship Some
Lymphatic malformation Is a Disorders of lymph node and lymphatics false Inferred relationship Some
Lymphatic malformation Finding site Structure of lymphatic vessel true Inferred relationship Some 1
Lymphatic malformation Is a Congenital malformation false Inferred relationship Some
Lymphatic malformation Occurrence Congenital false Inferred relationship Some
Lymphatic malformation Finding site Lymphatic tissue false Inferred relationship Some
Lymphatic malformation Associated morphology Congenital lymphatic malformation (morphologic abnormality) false Inferred relationship Some 1
Lymphatic malformation Is a Mass of body structure false Inferred relationship Some
Lymphatic malformation Is a Congenital malformation true Inferred relationship Some
Lymphatic malformation Occurrence Congenital false Inferred relationship Some
Lymphatic malformation Is a Lesion of soft tissue (disorder) false Inferred relationship Some
Lymphatic malformation Associated morphology Congenital lymphatic malformation (morphologic abnormality) false Inferred relationship Some 1
Lymphatic malformation Finding site Structure of lymphatic vessel false Inferred relationship Some 1
Lymphatic malformation Occurrence Congenital false Inferred relationship Some 2
Lymphatic malformation Associated morphology anomalie du développement false Inferred relationship Some 2
Lymphatic malformation Finding site Structure of lymphatic vessel false Inferred relationship Some 2
Lymphatic malformation Occurrence Congenital true Inferred relationship Some 1
Lymphatic malformation Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Lymphatic malformation Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Arteriovenous-lymphatic malformation Is a True Lymphatic malformation Inferred relationship Some
Acquired lymphangioma Is a False Lymphatic malformation Inferred relationship Some
Congenital lymphangioma Is a True Lymphatic malformation Inferred relationship Some
Hereditary edema of legs Is a False Lymphatic malformation Inferred relationship Some
Congenital malformation of lymphatic vessel of skin (disorder) Is a True Lymphatic malformation Inferred relationship Some
Venous-lymphatic malformation Is a True Lymphatic malformation Inferred relationship Some
Diffuse lymphatic malformation (disorder) Is a True Lymphatic malformation Inferred relationship Some
A rare, complex, vascular malformation syndrome characterized by capillary malformation of the lower lip, lymphatic malformation of the face and neck, asymmetry of face and limbs, and partial or generalized overgrowth involving one or more body segments. Is a True Lymphatic malformation Inferred relationship Some
A rare genetic disease characterized by the presence of Müllerian duct derivatives (rudimentary uterus, fallopian tubes, and atretic vagina) and other genital anomalies (cryptorchidism, micropenis) in male newborns, intestinal and pulmonary lymphangiectasia, protein-losing enteropathy, hepatomegaly, and renal anomalies. Postaxial polydactyly, facial dysmorphism (including broad nasal bridge, bulbous nasal tip, long and prominent upper lip with smooth philtrum, hypertrophic alveolar ridges, and mild retrognathia, among other features), and short limbs have also been described. The syndrome is fatal in infancy. Is a False Lymphatic malformation Inferred relationship Some
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to intestinal lymphangiectasia. There have been no further descriptions in the literature since 1985. Is a False Lymphatic malformation Inferred relationship Some
Congenital lymphangiectasia Is a True Lymphatic malformation Inferred relationship Some
Percutaneous sclerotherapy of lymphatic malformation using fluoroscopic guidance (procedure) Has focus True Lymphatic malformation Inferred relationship Some 3
Lymphangiomatosis (disorder) Is a True Lymphatic malformation Inferred relationship Some
A rare lymphatic system anomaly characterized by multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract, and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically, the lesions appear as round to oval, red-brown plaques, as large as a few centimeters in diameter. Histopathologically, they consist of dilated, thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers, and resembling benign lymphangioendothelioma. Is a True Lymphatic malformation Inferred relationship Some
A rare common cystic lymphatic malformation characterized by a benign cystic lesion composed of dilated lymphatic channels. Mixed cystic lesions consist of cysts both larger (macrocystic) and smaller (microcystic) than 1 cm in diameter. They usually present at birth or during the first years of life and most often occur in the head and neck region but may affect any site. Symptoms depend on the location and extent of the lesion. Infection, trauma, or intracystic hemorrhage can lead to lesional expansion. Malignant transformation does not occur. Is a True Lymphatic malformation Inferred relationship Some
Aplasia of lymphatic vessel Is a True Lymphatic malformation Inferred relationship Some

This concept is not in any reference sets

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