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61685007: 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:

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

5052 descendants. Search Descendants:

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
MT-ATP6-related mitochondrial spastic paraplegia Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive spastic paraplegia type 27 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 69 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 60 is a rare, complex hereditary spastic paraplegia disorder with characteristics of infantile onset of progressive lower limb spasticity, inability to walk, hypertonia and impaired vibration sense at ankles, with complicating signs including sensory impairment, nystagmus, motor axonal neuropathy and mild intellectual disability. Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 3 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Open wound of lower limb with tendon involvement Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 14 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Superficial injury of lower leg with infection Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
CT of pelvis and lower limb with contrast Procedure site - Direct (attribute) True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 8 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 66 is a rare, complex hereditary spastic paraplegia disorder with characteristics of infantile onset of progressive lower limb spasticity, severe gait disturbances leading to a non-ambulatory state, absent deep tendon reflexes and amyotrophy. Additional signs include severe sensorimotor neuropathy, pes equinovarus and mild intellectual disability. Cerebellar and corpus callosum hypoplasia, as well as colpocephaly, are observed on neuroimaging. Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 38 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 56 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 24 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 71 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal spastic paraplegia type 72 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked spastic paraplegia type 16 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 13 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Ulcer of lower limb due to type 1 diabetes mellitus (disorder) Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Neurofibroma of lower limb Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
SPOAN and SPOAN-related disorder Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Amputated lower limb (finding) Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Cone beam CT guided insertion of drain into lower limb Procedure site - Direct (attribute) True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Constriction ring syndrome of lower limb with amputation Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic paraplegia with precocious puberty syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic neurogenic ulcer of lower limb Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic neurogenic ulcer of lower limb Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Lymphedematous hyperkeratosis Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Groin mass (finding) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Crushing injuries involving multiple regions of upper limb(s) with lower limb(s) Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Lower limb of fetus palpable vaginally (finding) Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Sirenomelus (disorder) Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Foreign body in skin of lower limb with infection (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Open wounds involving multiple regions of upper limb(s) with lower limb(s) Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Intrauterine amputation of lower limb (disorder) Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Limb pain at rest due to atherosclerosis of artery of lower limb Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal sirenomelia Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Endoscopic procedure of lower limb (procedure) Procedure site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Unequal lower limb length due to acquired shortening of left femur (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Unequal lower limb length due to acquired shortening of right femur (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Unequal lower limb length due to acquired shortening of left tibia Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Unequal lower limb length due to acquired shortening of right tibia (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked complex hereditary spastic paraplegia Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked pure hereditary spastic paraplegia Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Painful legs and moving toes Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Application of hip spica cast Procedure site - Indirect (attribute) False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ober-Yount fasciotomy, combined with spica cast, pins in tibia and wedging the cast Procedure site - Indirect (attribute) True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Hodgkin's disease of lymph nodes of inguinal region AND/OR lower limb Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare complex hereditary spastic paraplegia characterised by neonatal to infantile onset of progressive spasticity in the lower limbs, hyperreflexia, tip-toe walking, pes equinus, and delayed motor developmental milestones. Kyphoscoliosis becomes evident in older patients, and most patients show atrophy of the lateral aspects of the tongue. Additional signs may include intellectual disability, language impairment, and moderate upper limb involvement. Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive spastic paraplegia type 76 is a rare, complex hereditary spastic paraplegia characterized by adult onset slowly progressive, mild to moderate lower limb spasticity and hyperreflexia, resulting in gait disturbances, commonly associated with upper limb hyperreflexia and dysarthria. Foot deformities (usually pes cavus) and extensor plantar responses are also frequent. Additional features may include ataxia, lower limb weakness/amyotrophy, abnormal bladder function, distal sensory loss and mild intellectual deterioration. Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Allan-Herndon-Dudley syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 5
Autosomal recessive spastic paraplegia type 78 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Drainage of lower limb using computed tomography guidance (procedure) Procedure site - Direct (attribute) True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive spastic paraplegia type 74 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 5
X-linked hereditary spastic paraplegia (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive hereditary spastic paraplegia Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Complicated hereditary spastic paraplegia (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive spastic paraplegia type 48 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive spastic paraplegia type 5A Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
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) 3
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) 3
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) 3
Autosomal recessive spastic paraplegia type 45 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary sensory and autonomic neuropathy with spastic paraplegia Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Spastic paraplegia with Paget disease of bone syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive spastic paraplegia type 27 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Allan-Herndon-Dudley syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 6
X-linked spastic paraplegia type 2 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
X-linked complex hereditary spastic paraplegia 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) 3
Autosomal recessive spastic paraplegia type 57 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
MT-ATP6-related mitochondrial spastic paraplegia Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 12 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 19 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive spastic paraplegia type 28 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Spastic paraplegia, facial cutaneous lesion syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
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) 2
Autosomal dominant spastic paraplegia type 42 (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
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) 2
Spastic paraplegia, glaucoma, intellectual disability syndrome (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Spastic paraplegia with precocious puberty syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic paraplegia, nephritis, deafness syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Intellectual disability, spasticity, ectrodactyly syndrome Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal dominant spastic paraplegia type 9A Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant spastic paraplegia type 9B (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare complex hereditary spastic paraplegia characterized by early onset of slowly progressive spastic para- or tetraparesis, increased tendon reflexes, positive Babinski sign, global developmental delay, cognitive impairment, and pseudobulbar palsy. Additional manifestations include dysmorphic facial features, tremor, short stature, and urinary incontinence. Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant spastic paraplegia type 73 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive spastic paraplegia type 75 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive spastic paraplegia type 77 Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Transplantation of muscle flap to lower extremity Procedure site - Direct (attribute) True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 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. Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple injuries of lower limb Finding site True Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Unequal lower limb length due to acquired shortening of left fibula Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Unequal lower limb length due to acquired shortening of right fibula (disorder) Finding site False Lower limb structure (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital deformity of lower limb (disorder) Finding site True 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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