| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Tendinosis of bilateral shoulders |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Tendinosis of bilateral shoulders |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
4 |
| Acquired hypoganglionosis of large intestine |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Acquired hypoganglionosis of large intestine |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
4 |
| Autosomal dominant hereditary spastic paraplegia |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Subconjunctival degeneration |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Degeneration of posterior pole of eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Miner's knee |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Tendinosis of right knee |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Tendinosis of left knee |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Degeneration of spine |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Lipodermatosclerosis of lower limb due to varicose veins of lower limb |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
12 |
| Autosomal dominant spastic paraplegia type 31 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal spastic paraplegia type 30 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Spastic paraplegia, facial cutaneous lesion syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Actinic cheilitis |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Osteoarthritis of midtarsal joints of bilateral feet |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive spastic paraplegia type 35 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive spastic paraplegia type 62 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Spinocerebellar ataxia with axonal neuropathy type 1 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive spastic paraplegia type 43 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Spinocerebellar ataxia with axonal neuropathy type 1 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 5A |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 21 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Osteoarthritis of midtarsal joints of bilateral feet |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant spastic paraplegia type 19 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Spastic paraplegia, neuropathy, poikiloderma syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked spastic paraplegia type 34 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Primary essential cutis verticis gyrata |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 15 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 48 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant spastic paraplegia type 41 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant spastic paraplegia type 42 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant spastic paraplegia type 12 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Hypotonia, speech impairment, severe cognitive delay syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 28 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant spastic paraplegia type 37 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Degenerative rupture of lateral meniscus of bilateral knees |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
4 |
| Degenerative rupture of lateral meniscus of bilateral knees |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 45 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 67 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Mixed dementia |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Acquired hypoganglionosis of large intestine |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Acquired hypoganglionosis of large intestine |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary hollow viscus myopathy |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant spastic paraplegia type 17 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Band keratopathy of right eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Band keratopathy of bilateral eyes |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Band keratopathy of bilateral eyes |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Band keratopathy of left eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Degenerative progressive high myopia of bilateral eyes |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Degenerative progressive high myopia of bilateral eyes |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Degenerative progressive high myopia of left eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Nodular degeneration of bilateral corneas |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Nodular degeneration of bilateral corneas |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Nodular degeneration of left cornea |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Myopic macular degeneration of left eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Myopic macular degeneration of right eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Degenerative progressive high myopia of right eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Nodular degeneration of right cornea |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 58 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive spastic paraplegia type 70 |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Pinguecula of bilateral eyes |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant neovascular inflammatory vitreoretinopathy |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Pinguecula of left eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Vitreous degeneration of right eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Vitreous degeneration of left eye |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Vitreous degeneration of bilateral eyes |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Vitreous degeneration of bilateral eyes |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Lattice degeneration of right retina |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Lattice degeneration of right retina |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Lattice degeneration of left retina |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Lattice degeneration of left retina |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Lattice degeneration of bilateral retinas |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Lattice degeneration of bilateral retinas |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
4 |
| Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Schisis of right retina |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Schisis of left retina |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Retinoschisis and retinal cysts |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Schisis of bilateral retinas |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Flat retinoschisis |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Aicardi's syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital degeneration of nervous system |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Schisis of bilateral retinas |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Spinocerebellar ataxia dysmorphism syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Spinocerebellar ataxia dysmorphism syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
4 |
| Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital chorioretinal degeneration |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Encephalopathy, intracerebral calcification, retinal degeneration syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Hypotrichosis with juvenile macular degeneration syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
3 |
| Van den Bosch syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Stickler syndrome |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Osteoarthritis of bilateral wrists |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Osteoarthritis of bilateral wrists |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |
| Osteoarthritis of bilateral shoulders |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
1 |
| Osteoarthritis of bilateral shoulders |
Associated morphology |
False |
Degeneration |
Inferred relationship |
Existential restriction modifier |
2 |