| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Hemiplegia of dominant side due to and following ischemic cerebrovascular accident | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Monoplegia of upper limb due to and following ischemic cerebrovascular accident | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Hemiplegia of nondominant side due to and following embolic cerebrovascular accident | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Paraplegia due to and following cerebrovascular accident | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Acute paralytic poliomyelitis, vaccine-associated | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Acute bulbar poliomyelitis caused by Human poliovirus 2 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Acute bulbar poliomyelitis caused by Human poliovirus 1 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Acute paralytic poliomyelitis caused by Human poliovirus 1 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Acute paralytic poliomyelitis caused by Human poliovirus 2 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Acute paralytic poliomyelitis caused by Human poliovirus 3 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Congenital fibrosis of inferior rectus muscle | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Severe intellectual disability and progressive spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 7 | 
| Autosomal recessive spastic paraplegia type 27 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal dominant spastic paraplegia type 3 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Severe intellectual disability, progressive spastic diplegia syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Autosomal recessive spastic paraplegia type 69 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 71 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal spastic paraplegia type 72 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 60 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 66 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Inherited congenital spastic tetraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Autosomal recessive spastic paraplegia type 14 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 9 | 
| Autosomal dominant spastic paraplegia type 38 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| X-linked spastic paraplegia type 16 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 2 | 
| Autosomal dominant spastic paraplegia type 13 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 56 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 24 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal dominant spastic paraplegia type 8 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Childhood-onset autosomal recessive myopathy with external ophthalmoplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 7 | 
| Progressive external ophthalmoplegia of bilateral eyes | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Hemiparesis of left side of face | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Hemiparesis of right side of face | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Autosomal dominant progressive external ophthalmoplegia type 5 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Autosomal dominant progressive external ophthalmoplegia type 3 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Autosomal dominant progressive external ophthalmoplegia type 4 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Autosomal dominant progressive external ophthalmoplegia type 1 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Autosomal dominant progressive external ophthalmoplegia type 2 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Atypical progressive supranuclear palsy syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| X-linked complex hereditary spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| X-linked pure hereditary spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Progressive supranuclear palsy corticobasal syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Progressive supranuclear palsy progressive non fluent aphasia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Exophthalmic ophthalmoplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Monoparesis of lower limb | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Paralytic syndrome on one side of the body as effect of cerebrovascular accident | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Ophthalmoplegia due to diabetes mellitus | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Hemiparesis as late effect of cerebrovascular disease | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Monoplegia of arm dominant side as sequela of cerebrovascular disease | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 7 | 
| Autosomal recessive spastic paraplegia type 76 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 8 | 
| Autosomal recessive spastic paraplegia type 74 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Hereditary spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 7 | 
| Spastic paraplegia, severe developmental delay, epilepsy syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 8 | 
| Autosomal dominant hereditary spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| X-linked hereditary spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Autosomal recessive hereditary spastic paraplegia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Autosomal dominant spastic paraplegia type 9B | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal dominant spastic paraplegia type 9A | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 9B | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal dominant spastic paraplegia type 73 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 75 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 77 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Autosomal recessive spastic paraplegia type 78 | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Lethal neonatal spasticity, epileptic encephalopathy syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Acquired horizontal gaze palsy | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Ophthalmoplegia due to abetalipoproteinemia | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Isolated acquired horizontal gaze palsy | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Congenital fibrosis syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Congenital horizontal gaze palsy | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Isolated congenital horizontal gaze paresis | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Intermittent horizontal conjugate gaze deviation | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Intermittent upward gaze deviation | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Horizontal gaze preference | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Ophthalmoplegia due to and following Guillain-Barré syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 6 | 
| Ophthalmoplegia due to neuropathy | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Paralysis of downgaze | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Paralysis of upgaze | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Combined paralysis of upgaze and downgaze | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Wall-eyed bilateral internuclear ophthalmoplegia syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Pseudoprogeria syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 10 | 
| Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 8 | 
| Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 8 | 
| Vertical one-and-a-half syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 7 | 
| NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 12 | 
| Periodic alternating gaze deviation | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Ophthalmoplegia due to phytanic acid storage disease | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 5 | 
| Sustained upward gaze deviation | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Sustained horizontal conjugate gaze deviation, contralateral type | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Sustained horizontal conjugate gaze deviation, ipsilateral type | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Sustained horizontal conjugate gaze deviation | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Paralytic shellfish poisoning | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 4 | 
| Aspergillus clavatus tremors | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Tremor due to substance withdrawal | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 2 | 
| Impairment of motor nerve function due to and following operation on skin | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 3 | 
| Bobble-head doll syndrome | Interprets | True | Movement | Inferred relationship | Existential restriction modifier | 1 |