30213001: Lymphatic edema (morphologic abnormality)

SNOMED CT Concept\Body structure\Body structure, altered from its original anatomical structure (morphologic abnormality)\Morphologically abnormal structure\Mechanical abnormality\Fluid disturbance\Edema\Lymphatic edema

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Lymphatic edema	Is a	Edema	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Correction of lymphedema by transplantation of autogenous lymphatics graft	Direct morphology	True	Lymphatic edema	Inferred relationship	Some	1
Kondoleon correction for lymphedema	Direct morphology	True	Lymphatic edema	Inferred relationship	Some	2
Excision of lymphoedematous tissue and full thickness skin graft	Direct morphology	False	Lymphatic edema	Inferred relationship	Some	3
Excision of lymphoedematous tissue plus local skin graft	Direct morphology	False	Lymphatic edema	Inferred relationship	Some	3
Malayan elephantiasis	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	4
Malayan elephantiasis	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	3
ikke-filariaforårsaget elephantiasis	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Chronic obstructive bancroftian filariasis	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	3
Bancroftian elephantiasis	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	3
Onchocercal elephantiasis	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
A rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies. Onset occurs during the first few weeks or months of life with hypotonia, poor feeding, drowsiness and abnormal movements. Infantile spasms, hypsarrhythmia and seizures appear during the first year of life. Visual loss, abnormal eye movements and optic atrophy also occur during infancy. Transmission appears to be autosomal recessive. A significant number of patients have been described who displayed most of the diagnostic criteria and features of PEHO syndrome, but did not appear to have cerebral atrophy on MRI, lacked the ophthalmologic signs and showed no reduction in CSF IGF-1 levels. This group of patients was diagnosed with PEHO-like syndrome. The prognosis is poor and most patients die before 15 years of age, mainly as a result of pneumonia or aspiration.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
PEHO-like syndrome is a rare, genetic neurological disease characterized by progressive encephalopathy, early-onset seizures with a hypsarrhythmic pattern, facial and limb edema, severe hypotonia, early arrest of psychomotor development and craniofacial dysmorphism (evolving microcephaly, narrow forehead, short nose, prominent auricles, open mouth, micrognathia), in the absence of neuro-ophthalmic or neuroradiologic findings. Poor visual responsiveness, growth failure and tapering fingers are also associated.	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Constriction ring of lower limb with lymphedema	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Elephantiasis of eyelid	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Bancroftian filarial fever	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Lymphatic filariasis	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Early bancroftian filariasis	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Bancroftian filarial abscess	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Acute Malayan filarial abscess	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
Elephantiasis of lower eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Infection by Brugia malayi	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Infection by Wuchereria bancrofti	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	2
Filarial abscess (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
Elephantiasis of upper eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Acute Malayan filariasis	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Malayan filarial fever (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Chronic Malayan filariasis	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Bancroftian filarial chylocele	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	4
Early bancroftian filariasis	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Infection by Brugia malayi	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Bancroftian filarial fever	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Infection by Wuchereria bancrofti	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Bancroftian filarial chylocele	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
Bancroftian filarial abscess	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Hennekam lymphangiectasia-lymphedema syndrome (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Emberger syndrome	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
Elephantiasis of eyelid	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Chronic obstructive bancroftian filariasis	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
Bancroftian elephantiasis	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphoedematous hyperkeratosis	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
Lymphedema due to chronic inflammation	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphedema due to recurrent infection	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphedema due to podoconiosis (disorder)	Associated morphology	True	Lymphatic edema	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	Lymphatic edema	Inferred relationship	Some	3
A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by global developmental delay, intellectual disability, macrothrombocytopenia, lymphedema, and dysmorphic facial features (like synophrys, ptosis, eversion of the lateral portion of the lower eyelid, and thin upper lip, among others). Additional reported manifestations include cardiac and genitourinary anomalies, sensorineural hearing loss, ophthalmologic abnormalities, skeletal anomalies, and immunodeficiency. Brain imaging may show enlarged ventricles, cerebellar atrophy, or white matter changes.	Associated morphology	False	Lymphatic edema	Inferred relationship	Some	5
A rare primary lymphoedema characterised by extensive, multisegmental lymphoedema, associated with persistent, widespread infections with various genital high- and low-risk human papillomaviruses, resulting in multifocal anogenital dysplasia. Laboratory examination shows abnormalities in lymphocyte subsets, in particular CD4+ T-cells. Epidermal naevi and capillary malformations have also been reported.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
A rare genetic disease characterised by choanal atresia and early onset of lymphoedema of the lower extremities. Additional reported features include facial dysmorphism (hypertelorism, broad forehead, smooth philtrum, unilateral low-set ear, and high-arched palate), hypoplastic nipples, and pectus excavatum.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Facial lymphedema due to acne	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Facial lymphoedema due to rosacea	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lipo-lymphoedema	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Primary lymphedema is a lymphatic system malformation characterized by swelling of an extremity that can be associated with other lymphatic effusions, due to an underlying developmental anomaly of the lymphatic system (abnormal lymphangiogenesis) It can be hereditary or not and be congenital or late onset.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by global developmental delay, intellectual disability, macrothrombocytopenia, lymphedema, and dysmorphic facial features (like synophrys, ptosis, eversion of the lateral portion of the lower eyelid, and thin upper lip, among others). Additional reported manifestations include cardiac and genitourinary anomalies, sensorineural hearing loss, ophthalmologic abnormalities, skeletal anomalies, and immunodeficiency. Brain imaging may show enlarged ventricles, cerebellar atrophy, or white matter changes.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	2
Primary lymphedema with systemic and visceral involvement	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Primary lymphoedema with systemic involvement	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Primary lymphoedema with visceral involvement	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Primary lymphedema due to syndrome (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
A rare primary lymphedema characterized by a highly variable lymphatic phenotype ranging from severe lymphatic-related hydrops fetalis, which may cause perinatal demise or fully resolve to become completely asymptomatic, to a mild presentation in older patients with persistent varicose veins, peripheral edema, and impaired lymph drainage in the lower limbs. Atrial septal defect has been described in association and may be the only anomaly in some patients.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
A rare genetic primary lymphedema characterized by uniform, widespread lymphedema, often with systemic involvement such as intestinal and pulmonary lymphangiectasia, pleural and pericardial effusions, and chylothorax. There is a high incidence of non-immune hydrops fetalis, which may result in fetal demise or fully resolve after birth. Severe, recurrent facial cellulitis is observed in some patients. Presence of epicanthic folds or micrognathia has occasionally been reported, while intelligence is normal, and seizures are absent.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
A rare genetic primary lymphoedema characterised by unilateral or bilateral lower limb lymphoedema of variable severity. The condition shows almost complete penetrance with onset in childhood or adolescence in females, whereas in males it shows incomplete penetrance with later onset of disease. Lymphoscintigraphy in more severely affected individuals reveals lymphatic abnormalities consistent with lymphangiectasia, valve dysfunction, and thoracic duct reflux.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
A rare primary lymphedema characterized by bilateral, painless lower limb swelling present at birth. Prominent veins around the ankles and on the dorsa of the feet, dysplastic and upslanting toenails due to edema of the nailbed, and subtle dysmorphic facial features (such as high forehead, hypertelorism, depressed nasal bridge, mild bilateral ear dysplasia, and short neck) have also been described. The degree of lymphatic impairment is milder than in the otherwise clinically similar Milroy disease, as evidenced by slightly less severe lymphedema and significantly more uptake of tracers on lymphoscintigraphy.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
A rare genetic primary lymphedema characterized by lymphedema of all four limbs with age of onset ranging from birth to adulthood. Manifestations are of variable severity, and upper limb involvement may develop only later in the disease course. Recurrent episodes of cellulitis and skin infections are observed in severe cases. Varicose veins and venous incompetence have been reported in association.	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Secondary paediatric lymphoedema	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphatic filariasis of right eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphatic filariasis of left upper eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphatic filariasis of left eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphatic filariasis of left lower eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphatic filariasis of right lower eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Lymphatic filariasis of right upper eyelid (disorder)	Associated morphology	True	Lymphatic edema	Inferred relationship	Some	1
Excision of lymphoedematous tissue and full thickness skin graft	Direct morphology	True	Lymphatic edema	Inferred relationship	Some	1
Excision of lymphedematous tissue and split thickness graft of skin (procedure)	Direct morphology	True	Lymphatic edema	Inferred relationship	Some	1
Excision of lymphoedematous tissue plus local skin graft	Direct morphology	True	Lymphatic edema	Inferred relationship	Some	1

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Id	Description	Lang	Type	Status	Case?	Module
50557011	Lymphatic edema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
50558018	Acquired lymphedema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
50561017	Lymphedema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
484517014	Acquired lymphoedema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
484518016	Lymphatic oedema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
484519012	Lymphoedema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
761193017	Lymphatic edema (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2617451000005113	lymfatisk ødem	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)