61685007: Lower limb structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\Body region structure\...

\Structure of half of body lateral to midsagittal plane\Limb structure\Lower limb structure (body structure)

\Body part structure\Lower body structure (body structure)\Lower body part structure\Structure of pelvic cross-sectional segment of trunk and/or lower limb (body structure)\Lower limb structure (body structure)
\Body part structure\Limb structure\Lower limb structure (body structure)

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
Lower limb structure (body structure)	Is a	Limb structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Lower limb structure (body structure)	partie de	Entire body as a whole (body structure)	false	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Lower limb structure (body structure)	Is a	Pelvis and/or lower extremity structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Lower limb structure (body structure)	Laterality	Side	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Lower limb structure (body structure)	Is a	Lower body part structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Lower limb structure (body structure)	Is a	Structure of pelvic cross-sectional segment of trunk and/or lower limb (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Dipygus	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Gastrothoracopagus dipygus	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Sirenomelus (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	3
X-ray tomography of lower limb	Procedure site - Direct (attribute)	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Paraplegia, brachydactyly, cone-shaped epiphysis syndrome	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Gastrothoracopagus dipygus	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Problem of lower limb	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Functional paraparesis (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
X-linked hereditary spastic paraplegia (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 32 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 26 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 23	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 64 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 63 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 61	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Spastic paraplegia with Paget disease of bone syndrome	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare disorder characterized by the absence of the upper limbs and severe underdevelopment of the lower limbs. Minor facial abnormalities (depressed nasal root, upturned nose, infra-orbital creases, prominent cheeks and micrognathia) were also reported. The syndrome has been described in three fetuses born to non-consanguineous parents.	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 18 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 25 (SPG25) is a rare, complex type of hereditary spastic paraplegia characterized by adult-onset spastic paraplegia associated with spinal pain that radiates to the upper or lower limbs and is related to disc herniation (with minor spondylosis), as well as mild sensorimotor neuropathy. The SPG25 phenotype has been mapped to a locus on chromosome 6q23-q24.1.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 10 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 6	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 29	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)
Spastic paraplegia with precocious puberty syndrome	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Spastic paraplegia, glaucoma, intellectual disability syndrome (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Spastic paraplegia, nephritis, deafness syndrome	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	9
Flaccid monoplegia of lower limb (disorder)	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Monoplegia of lower limb as sequela of cerebrovascular accident	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Paraplegia due to and following cerebrovascular accident (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Autosomal dominant hereditary spastic paraplegia	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Absence of lower limb due to diabetes mellitus	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Complex burn of lower limb (disorder)	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal dominant spastic paraplegia type 4 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal dominant spastic paraplegia type 10 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal dominant spastic paraplegia type 6	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
X-linked hereditary spastic paraplegia (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal recessive spastic paraplegia type 48 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 5A	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A complex hereditary spastic paraplegia characterised by progressive lower limbs weakness and spasticity, upper limbs weakness, dysarthria, hypomimia, sphincter disturbances, peripheral neuropathy, learning difficulties, cognitive impairment and dementia. Magnetic resonance imaging shows thin corpus callosum, cerebral atrophy, and periventricular white matter changes.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary sensory and autonomic neuropathy with spastic paraplegia	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 39	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal dominant spastic paraplegia type 36	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 44 (SPG44) is a very rare, complex form of hereditary spastic paraplegia characterized by a late-onset, slowly progressive spastic paraplegia associated with mild ataxia and dysarthria, upper extremity involvement (i.e. loss of finger dexterity, dysmetria), and mild cognitive impairment, without the presence of nystagmus. A hypomyelinating leukodystrophy and thin corpus callosum is observed in all cases and psychomotor development is normal or near normal. SPG44 is caused by mutations in the GJC2 gene (1q41-q42) encoding the gap junction gamma-2 protein.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 46 (SPG46) is a rare, complex type of hereditary spastic paraplegia characterised by an onset, in infancy or childhood, of the typical signs of spastic paraplegia (i.e. spastic gait and weakness of the lower limbs) associated with a variety of additional manifestations including upper limb spasticity and weakness, pseudobulbar dysarthria, bladder dysfunction, cerebellar ataxia, cataracts, and cognitive impairment that can progress to dementia. Brain imaging may show thinning of the corpus callosum and mild atrophy of the cerebrum and cerebellum. SPG46 is due to mutations in the GBA2 gene (9p13.2) encoding non-lysosomal glucosylceramidase.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 53 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 54 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 55 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 57	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 32 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 26 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 23	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 64 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 63 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 61	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spastic paraplegia with Paget disease of bone syndrome	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 18 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 25 (SPG25) is a rare, complex type of hereditary spastic paraplegia characterized by adult-onset spastic paraplegia associated with spinal pain that radiates to the upper or lower limbs and is related to disc herniation (with minor spondylosis), as well as mild sensorimotor neuropathy. The SPG25 phenotype has been mapped to a locus on chromosome 6q23-q24.1.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal dominant spastic paraplegia type 29	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 15 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 21	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 43 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Normal lower limb movement and sensation and circulation (finding)	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Complicated hereditary spastic paraplegia (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal dominant spastic paraplegia type 19 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
X-linked spastic paraplegia type 34	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 35 is a rare form of hereditary spastic paraplegia characterized by childhood (exceptionally adolescent) onset of a complex phenotype presenting with lower limb (followed by upper limb) spasticity with hyperreflexia and extensor plantar responses, with additional manifestations including progressive dysarthria, dystonia, mild cognitive decline, extrapyramidal features, optic atrophy and seizures. White matter abnormalities and brain iron accumulation have also been observed on brain magnetic resonance imaging.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare type of hereditary spastic paraplegia usually characterized by a pure phenotype of proximal weakness of the lower extremities with spastic gait and brisk reflexes, with a bimodal age of onset of either childhood or adulthood (>30 years). In some cases, it can present as a complex phenotype with additional associated manifestations including peripheral neuropathy, bulbar palsy (with dysarthria and dysphagia), distal amyotrophy, and impaired distal vibration sense.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spastic paraplegia, facial cutaneous lesion syndrome	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A pure form of hereditary spastic paraplegia characterized by onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal dominant spastic paraplegia type 42 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal dominant spastic paraplegia type 12 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal recessive spastic paraplegia type 28	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Intellectual disability, spasticity, ectrodactyly syndrome	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A pure or complex form of hereditary spastic paraplegia characterized by an onset in the first decade of life of spastic paraparesis (more prominent in lower than upper extremities) and unsteady gait, as well as increased deep tendon reflexes, amyotrophy, cerebellar ataxia, and flexion contractures of the knees, in some.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare, pure or complex form of hereditary spastic paraplegia characterised by either a pure spastic paraplegia phenotype, usually presenting in the first or second decade of life, with spastic lower extremities, unsteady spastic gait, hyperreflexia and extensor plantar responses, or as a complicated phenotype with the additional manifestations of distal wasting, saccadic ocular movements, mild cerebellar ataxia and mild, distal, axonal neuropathy.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A pure form of hereditary spastic paraplegia characterised by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients.	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal recessive spastic paraplegia type 45 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 67 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
inégalité acquise de la longueur des membres inférieurs	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Lower limb malformation hypospadias syndrome	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal dominant spastic paraplegia type 17 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 58	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive spastic paraplegia type 70 (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Dipygus	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Painful and cold lower limb	Finding site	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Needle stick injury of thigh	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Needle stick injury of knee (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Needle stick injury of lower leg	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Needle stick injury of calf	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Needle stick injury of ankle	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Needle stick injury of buttock	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Needle stick injury of hip (disorder)	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
MRI of pelvis and lower extremity	Procedure site - Direct (attribute)	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Computed tomography of abdomen, pelvis and lower limb (procedure)	Procedure site - Direct (attribute)	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
CT of pelvis and lower limb	Procedure site - Direct (attribute)	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
CT of abdomen, pelvis and lower limb with contrast	Procedure site - Direct (attribute)	True	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Autosomal recessive spastic paraplegia type 59	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Severe intellectual disability and progressive spastic paraplegia	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
MT-ATP6-related mitochondrial spastic paraplegia	Finding site	False	Lower limb structure (body structure)	Inferred relationship	Existential restriction modifier (core metadata concept)	1

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
102491013	Lower extremity	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
102495016	Lower limb	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
499092014	Lower limb structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
499093016	Lower extremity structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
800774010	Lower limb structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2552388018	Leg	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3756598010	Body structure that includes the hip, thigh, leg, ankle and foot.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
102491013	Lower extremity	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
102491013	Lower extremity	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
102495016	Lower limb	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
102495016	Lower limb	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
499092014	Lower limb structure	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499092014	Lower limb structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
499093016	Lower extremity structure	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499093016	Lower extremity structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
800774010	Lower limb structure (body structure)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
800774010	Lower limb structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2552388018	Leg	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2552388018	Leg	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2884699015	Lower extremity, including hip, thigh, leg, ankle, and foot	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3756598010	Body structure that includes the hip, thigh, leg, ankle and foot.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
886771000172119	structure du membre inférieur	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
903651000172116	membrum inferius	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1015421000172119	membre inférieur	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
886771000172119	structure du membre inférieur	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
903651000172116	membrum inferius	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1015421000172119	membre inférieur	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module