Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Spastic paraplegia with Paget disease of bone syndrome |
Associated morphology |
False |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 18 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 25 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant spastic paraplegia type 10 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant spastic paraplegia type 6 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spastic paraplegia with precocious puberty syndrome |
Associated morphology |
False |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant spastic paraplegia type 29 |
Associated morphology |
False |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia dysmorphism syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
3 |
Spinocerebellar ataxia dysmorphism syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
4 |
Encephalopathy, intracerebral calcification, retinal degeneration syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic paraplegia, nephritis, deafness syndrome |
Associated morphology |
False |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
5 |
Van den Bosch syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive cerebelloparenchymal disorder type 3 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal recessive cerebelloparenchymal disorder type 3 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
4 |
Richards-Rundle syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Richards-Rundle syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
3 |
Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal recessive spastic paraplegia type 11 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spastic paraparesis co-occurrent with deafness |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Cochleosaccular degeneration and cataract syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 7 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 7 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 1 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 1 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 2 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 2 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 6 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 6 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 8 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 8 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 10 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 10 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 4 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 4 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spastic paraplegia type 7 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 28 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 28 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 29 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 29 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 31 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 31 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Macrocephaly with spastic paraplegia and dysmorphism syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Primary progressive non fluent aphasia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Primary progressive non fluent aphasia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Logopenic progressive aphasia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Logopenic progressive aphasia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Right temporal atrophy variant frontotemporal dementia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 15/16 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 15/16 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Behavioral variant of frontotemporal dementia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Behavioral variant of frontotemporal dementia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Maternally inherited Leigh syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Infantile striatonigral degeneration |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital lactic acidosis Saguenay-Lac-Saint-Jean type |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Oligoosteoarthritis |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Prolapse of cervical intervertebral disc co-occurrent and due to degeneration |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Degeneration of cervical intervertebral disc co-occurrent with osteophyte of cervical vertebra |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Degeneration of thoracic intervertebral disc without prolapse |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Prolapse of thoracic intervertebral disc co-occurrent and due to degeneration |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Degeneration of thoracic intervertebral disc co-occurrent with osteophyte |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Degeneration of lumbar intervertebral disc without prolapse |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Prolapse of lumbar intervertebral disc co-occurrent and due to degeneration |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Degeneration of lumbar intervertebral disc co-occurrent with osteophyte of lumbar vertebra |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Osteoarthritis of joint of left ankle and/or foot |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Acquired hypoganglionosis of large intestine |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Acquired hypoganglionosis of large intestine |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant hereditary spastic paraplegia |
Associated morphology |
False |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Subconjunctival degeneration |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Degeneration of posterior pole of eye |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Degeneration of iris |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spastic paraplegia, glaucoma, intellectual disability syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
4 |
Spinocerebellar ataxia type 40 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 40 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia type 38 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia type 38 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Degeneration of spine |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Osteoarthritis of facet joint of thoracic spine |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Osteoarthritis of lumbar spinal facet joint |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Lumbosacral spondylosis co-occurrent with root compression |
Associated morphology |
False |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Severe intellectual disability and progressive spastic paraplegia |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 27 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Primary non-essential cutis verticis gyrata |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia |
Associated morphology |
False |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant spastic paraplegia type 3 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Gemignani syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Circumferential viscodilation and tensioning of sinus venosus of sclera by external approach |
Procedure morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 69 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 71 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal spastic paraplegia type 72 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 60 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 66 |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Infantile cerebellar and retinal degeneration |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
1 |
Infantile cerebellar and retinal degeneration |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal recessive cerebellar ataxia, psychomotor delay syndrome |
Associated morphology |
True |
Degenerative abnormality |
Inferred relationship |
Existential restriction modifier |
2 |