Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Spinal dislocation with lumbar cord lesion |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Fracture dislocation of thoracolumbar junction |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Injury of lumbar spinal cord (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Incomplete cord syndrome of lumbar spinal cord (disorder) |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
In a transitional lipoma of the spinal cord the lipoma-spinal cord interface includes the conus medullaris and extends to the dorsal and caudal aspects of the lumbar spinal cord. |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Caudal regression syndrome |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Myelopathy of thoracolumbar spine due to disc disorder (disorder) |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Lumbar radiculitis |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Lumbosacral agenesis (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
A rare, genetic, developmental defect during embryogenesis disorder characterized by varying degrees of caudal dysgenesis, ranging from a single umbilical artery or imperforate anus to full sirenomelia, in several members of the same family. Phenotype includes lumbosacral agenesis, anal atresia or ectopia, genitourinary abnormalities, components of VATER or VACTERL association, and facial dysmorphism (flat facies, abnormal ears, bilateral epicanthic folds, depressed nasal bridge, micrognathia). Additional features reported include cardiovascular (e.g. endocardial cushion defect, hypoplasia of pulmonary artery) and skeletal (kyphosis, hemipelvis) anomalies. |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Congenital deformity of lumbosacral joint |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Juvenile osteochondrosis of thoracolumbar spine (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Lumbosacral spondylosis |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Hydrocephaly-tall stature-joint laxity syndrome is a multiple congenital anomalies syndrome described in two sisters and characterized by the presence of hydrocephalus (onset in infancy), tall stature, joint laxity, and thoracolumbar kyphosis. There have been no further descriptions in the literature since 1989. |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Injury of lumbar nerve root (disorder) |
Is a |
False |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Adult osteochondrosis of thoracolumbar spine (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Disorder of enthesis of lumbar spine region (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Baastrup disease of lumbar spine (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Thoracolumbar postural kyphosis |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Lesion of lumbar spine |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Lumbar discogenic pain (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Traumatic injury of lumbar vertebral column region (disorder) |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|
Chronic primary low back pain |
Is a |
True |
Disorder of lumbar spine |
Inferred relationship |
Some |
|