Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Diplegic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Athetoid cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Facial palsy as birth trauma |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Monoplegic cerebral palsy affecting upper limb |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Monoplegic cerebral palsy affecting lower limb |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Dyskinetic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Ataxic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Paraplegic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Non-spastic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Dystonic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Choreic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Chorea-athetoid cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Mixed cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Bilateral cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Triplegic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Pentaplegic cerebral palsy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Horizontal gaze palsy with progressive scoliosis |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Paralytic syndrome of two limbs |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Paralytic syndrome of three limbs |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Paralytic syndrome on both sides of the body |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Infantile ascending hereditary spastic paralysis |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Ophthalmoplegia due to Graves' disease |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Acute paralytic poliomyelitis |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal recessive spastic paraplegia type 58 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 70 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Spinal atrophy, ophthalmoplegia, pyramidal syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Erb Duchenne palsy with neuroma due to birth trauma |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
7 |
Autosomal dominant spastic paraplegia type 31 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant spastic paraplegia type 41 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant spastic paraplegia type 42 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive spastic paraplegia type 48 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal dominant spastic paraplegia type 37 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
X-linked spastic paraplegia type 34 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Autosomal recessive spastic paraplegia type 5A |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal dominant spastic paraplegia type 12 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant spastic paraplegia type 19 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive spastic paraplegia type 28 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal spastic paraplegia type 30 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Spastic paraplegia, neuropathy, poikiloderma syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic paraplegia, facial cutaneous lesion syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 15 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 35 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
6 |
Autosomal recessive spastic paraplegia type 21 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 43 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 62 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 45 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 67 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Benign nocturnal alternating hemiplegia of childhood |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive spastic paraplegia type 59 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal dominant progressive external ophthalmoplegia |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive progressive external ophthalmoplegia |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
External ophthalmoplegia |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Progressive external ophthalmoplegia |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Hereditary sensory and autonomic neuropathy with spastic paraplegia |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
7 |
Autosomal recessive spastic paraplegia type 39 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
10 |
Flaccid diplegia of upper limbs |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic diplegia of upper limbs |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Diplegia of lower limbs |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic monoplegia of upper limb |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic monoplegia of lower limb |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Erb Duchenne palsy with neuropraxis due to traction birth trauma |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Macrostomia, preauricular tag, external ophthalmoplegia syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
6 |
X-linked spastic paraplegia type 2 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
7 |
Autosomal dominant spastic paraplegia type 36 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant spastic paraplegia type 4 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive spastic paraplegia type 44 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 46 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 53 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 54 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 55 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal recessive spastic paraplegia type 57 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
6 |
Functional monoparesis |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Functional paraparesis |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Functional hemiparesis |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Spastic paraplegia, optic atrophy, neuropathy syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
6 |
Autosomal recessive spastic paraplegia type 32 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 26 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 23 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 64 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 63 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 61 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Spastic paraplegia with Paget disease of bone syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 18 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive spastic paraplegia type 25 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal dominant spastic paraplegia type 10 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant spastic paraplegia type 6 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic paraplegia with precocious puberty syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal dominant spastic paraplegia type 29 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic paraplegia, nephritis, deafness syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive spastic paraplegia type 11 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |
Spastic paraplegia type 7 |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
5 |
Macrocephaly with spastic paraplegia and dysmorphism syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
7 |
Congenital suprabulbar paresis |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
3 |
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
6 |
Mitochondrial neurogastrointestinal encephalomyopathy syndrome |
Has interpretation |
True |
Absent |
Inferred relationship |
Existential restriction modifier |
4 |