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48087001: Lymphangiectasis (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
80136015 Lymphangiectasis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
80139010 Lymphangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
785616012 Lymphangiectasis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lymphangiectasis Is a Aneurysm true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Focal lymphangiectasis Is a True Lymphangiectasis Inferred relationship Some
Diffuse lymphangiectasis (morphologic abnormality) Is a True Lymphangiectasis Inferred relationship Some
Generalized lymphangiectasis Is a True Lymphangiectasis Inferred relationship Some
Congenital pulmonary lymphangiectasis Associated morphology False Lymphangiectasis Inferred relationship Some
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 1
Intestinal lymphangiectasis Associated morphology False Lymphangiectasis Inferred relationship Some 1
Conjunctival lymphangiectasis Associated morphology False Lymphangiectasis Inferred relationship Some 1
Hennekam lymphangiectasia-lymphedema syndrome (disorder) Associated morphology True Lymphangiectasis Inferred relationship Some 2
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 2
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 1
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 2
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 1
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 2
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 1
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 2
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 1
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 2
Primary lymphangiectasis of intestine (disorder) Associated morphology True Lymphangiectasis Inferred relationship Some 2
Primary lymphangiectasis of intestine (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 1
Conjunctival lymphangiectasis Associated morphology True Lymphangiectasis Inferred relationship Some 1
Intestinal lymphangiectasis Associated morphology True Lymphangiectasis Inferred relationship Some 1
Congenital pulmonary lymphangiectasis Associated morphology False Lymphangiectasis Inferred relationship Some 5
Congenital primary pulmonary lymphangiectasis (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 2
Congenital secondary pulmonary lymphangiectasis (disorder) Associated morphology False Lymphangiectasis Inferred relationship Some 2
Secondary intestinal lymphangiectasia Associated morphology False Lymphangiectasis Inferred relationship Some 1
Secondary intestinal lymphangiectasia is an acquired from of intestinal lymphangiectasia manifesting as a protein-losing enteropathy due to another disorder such as Crohn's disease, congestive heart failure, sarcoidosis, Turner syndrome and often in patients who have undergone a Fontan operation. It is characterised by malabsorption, diarrhoea, oedema due hypoproteinaemia, steatorrhoea and serosal effusions. Associated morphology True Lymphangiectasis Inferred relationship Some 1
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. Associated morphology False Lymphangiectasis Inferred relationship Some 3
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. Associated morphology False Lymphangiectasis Inferred relationship Some 4
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. Associated morphology True Lymphangiectasis Inferred relationship Some 1
Congenital pulmonary lymphangiectasis Associated morphology False Lymphangiectasis Inferred relationship Some 2
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. Associated morphology True Lymphangiectasis Inferred relationship Some 2
Congenital primary pulmonary lymphangiectasis (disorder) Associated morphology True Lymphangiectasis Inferred relationship Some 1
Congenital secondary pulmonary lymphangiectasis (disorder) Associated morphology True Lymphangiectasis Inferred relationship Some 1
Congenital pulmonary lymphangiectasis Associated morphology True Lymphangiectasis Inferred relationship Some 1
Acquired lymphangiectasia Associated morphology True Lymphangiectasis Inferred relationship Some 1
Congenital lymphangiectasia Associated morphology True Lymphangiectasis Inferred relationship Some 1
Acquired cutaneous lymphangiectasia Associated morphology True Lymphangiectasis Inferred relationship Some 1
Congenital cutaneous lymphangiectasia Associated morphology True Lymphangiectasis Inferred relationship Some 1
Congenital lymphangiectasia with chylous reflux (disorder) Associated morphology True Lymphangiectasis Inferred relationship Some 1
Acquired lymphangiectasia with chylous reflux Associated morphology True Lymphangiectasis Inferred relationship Some 1
Conjunctival lymphangiectasis Associated morphology False Lymphangiectasis Inferred relationship Some 2
Acquired cutaneous lymphangiectasia Associated morphology True Lymphangiectasis Inferred relationship Some 2
Congenital cutaneous lymphangiectasia Associated morphology False Lymphangiectasis Inferred relationship Some 2

Reference Sets

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