| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Spastic paraplegia, facial cutaneous lesion syndrome |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Intellectual disability, spasticity, ectrodactyly syndrome |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal recessive spastic paraplegia type 15 (disorder) |
Finding site |
True |
Structure of right lower limb (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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Autosomal recessive spastic paraplegia type 21 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 43 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| 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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Autosomal recessive spastic paraplegia type 45 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Autosomal recessive spastic paraplegia type 67 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 59 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| SPOAN and SPOAN-related disorder |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Hereditary sensory and autonomic neuropathy with spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Autosomal recessive spastic paraplegia type 39 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| X-linked spastic paraplegia type 2 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal dominant spastic paraplegia type 36 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal dominant spastic paraplegia type 4 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| 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 |
True |
Structure of right lower limb (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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 53 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 54 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 55 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
| Autosomal recessive spastic paraplegia type 57 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
| Functional paraparesis (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
| Autosomal recessive spastic paraplegia type 32 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 26 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 23 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 64 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 63 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 61 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Spastic paraplegia with Paget disease of bone syndrome |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Autosomal recessive spastic paraplegia type 18 (disorder) |
Finding site |
True |
Structure of right lower limb (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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal dominant spastic paraplegia type 10 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal dominant spastic paraplegia type 6 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal dominant spastic paraplegia type 29 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
| Spastic paraplegia, nephritis, deafness syndrome |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| 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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Spastic paraplegia type 7 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Fryns macrocephaly |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Spastic paraplegia, glaucoma, intellectual disability syndrome (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Paraplegia due to and following cerebrovascular accident (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
| Severe intellectual disability and progressive spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 27 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| MT-ATP6-related mitochondrial spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal dominant spastic paraplegia type 3 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal recessive spastic paraplegia type 69 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 71 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal spastic paraplegia type 72 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| 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 |
True |
Structure of right lower limb (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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 14 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Hereditary sensory and autonomic neuropathy due to TECPR2 mutation |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal dominant spastic paraplegia type 38 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| X-linked spastic paraplegia type 16 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Autosomal dominant spastic paraplegia type 13 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal recessive spastic paraplegia type 56 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Autosomal recessive spastic paraplegia type 24 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal dominant spastic paraplegia type 8 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| X-linked complex hereditary spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| X-linked pure hereditary spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| 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 |
True |
Structure of right lower limb (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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Autosomal recessive spastic paraplegia type 74 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
| Hereditary spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Autosomal dominant hereditary spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| X-linked hereditary spastic paraplegia (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Autosomal recessive hereditary spastic paraplegia |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Autosomal dominant spastic paraplegia type 9B (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal dominant spastic paraplegia type 9A |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| 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 |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Autosomal dominant spastic paraplegia type 73 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Autosomal recessive spastic paraplegia type 75 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Autosomal recessive spastic paraplegia type 77 |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Autosomal recessive spastic paraplegia type 78 (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Aspiration of right lower limb using ultrasonographic guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Fluoroscopy guided drainage of right lower extremity |
Procedure site - Indirect (attribute) |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Aspiration of bilateral lower limbs using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Drainage of bilateral lower limbs using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Aspiration of right lower limb using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Aspiration of bilateral lower limbs using ultrasonographic guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
12 |
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
| Spastic paraplegia with precocious puberty syndrome |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
| Autosomal dominant complex hereditary spastic paraplegia (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
| Injection of bilateral lower limbs using ultrasonographic guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Injection of bilateral lower limbs using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Injection of right lower limb using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Cellulitis of right lower limb (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Aspiration of right lower limb using fluoroscopic guidance (procedure) |
Procedure site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Aspiration of right lower limb using ultrasonographic guidance (procedure) |
Procedure site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Aspiration of bilateral lower limbs using ultrasonographic guidance (procedure) |
Procedure site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Aspiration of bilateral lower limbs using fluoroscopic guidance (procedure) |
Procedure site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Foreign body in right lower limb (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Bite wound of right lower limb (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Congenital arteriovenous malformation of bilateral lower limbs (disorder) |
Finding site |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Drainage of right lower limb using ultrasonographic guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of right lower limb (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
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