Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Insertion of adjustable suture into muscle of eye |
Procedure site - Indirect (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Excision of lesion of extraocular muscle |
Procedure site - Direct (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Shortening of extraocular muscle (procedure) |
Procedure site - Direct (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Shortening of extraocular muscles, two or more muscles (procedure) |
Procedure site - Direct (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Biopsy of extraocular muscle |
Procedure site - Direct (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Foville syndrome |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Foville's syndrome II |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Shortening procedure on one extraocular muscle |
Procedure site - Direct (attribute) |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Lengthening procedure on one extraocular muscle |
Procedure site - Direct (attribute) |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Revision of extraocular muscle surgery |
Procedure site - Direct (attribute) |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Revision of extraocular muscle surgery |
Procedure site - Direct (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Adjustment to extraocular muscle (procedure) |
Procedure site - Direct (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Entrapment of extraocular muscle (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Hypoplasia of eye muscle |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Vertical retraction syndrome |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
Congenital fibrosis of inferior rectus muscle (disorder) |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
Strabismus fixus |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
A rare syndromic disorder with strabismus with characteristics of congenital non-progressive ophthalmoplegia affecting the oculomotor and/or trochlear nucleus/nerve and their innervated muscles. Patients present with abnormal resting position of the eyes (in most cases infraducted and exotropic), limitation of vertical and horizontal gaze, impaired binocular vision, amblyopia, unilateral or bilateral blepharoptosis, and compensatory abnormal head posture. Extraocular manifestations include intellectual disability, peripheral neuropathy, and skeletal abnormalities among others. |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
Multiple supernumerary eye muscles |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Vertical retraction syndrome |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
4 |
Strabismus fixus |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
A rare syndromic disorder with strabismus with characteristics of congenital non-progressive ophthalmoplegia affecting the oculomotor and/or trochlear nucleus/nerve and their innervated muscles. Patients present with abnormal resting position of the eyes (in most cases infraducted and exotropic), limitation of vertical and horizontal gaze, impaired binocular vision, amblyopia, unilateral or bilateral blepharoptosis, and compensatory abnormal head posture. Extraocular manifestations include intellectual disability, peripheral neuropathy, and skeletal abnormalities among others. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Multiple supernumerary eye muscles |
Finding site |
False |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Hypoplasia of eye muscle |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Oculopharyngeal muscular dystrophy (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Oblique eye muscle structure |
Is a |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
|
Restrictive ophthalmopathy (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Thyroid eye disease |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
Rectus eye muscle structure |
Is a |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
|
External ophthalmoplegia |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Progressive external ophthalmoplegia |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Total ophthalmoplegia |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
A rare developmental defect during embryogenesis characterized by macrostomia or abnormal mouth contour, preauricular tags or pits, and uni- or bilateral ptosis due to external ophthalmoplegia. This syndrome belongs to the oculoauriculovertebral spectrum, a developmental disorder affecting the structures derived from the first and second branchial arches. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
4 |
A rare genetic neuromuscular disease characterized by early onset of proximal or generalized muscle weakness, external ophthalmoplegia with or without ptosis, and joint contractures. Hypotonia, neonatal respiratory distress necessitating ventilation, and severe dysphagia have also been reported. The disease is of variable severity and non- or slowly progressive. Patients typically remain ambulatory. Muscle biopsy may show predominance of type 1 fibers, marked variability in fiber size, increased internal nuclei, and proliferation of perimysial and endomysial connective tissue. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
5 |
A rare mitochondrial disease characterized by adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuropathy. Respiratory insufficiency has been reported in some cases. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
A rare mitochondrial disease characterized by adult onset of the triad of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis. Additional signs and symptoms are highly variable and include myopathy, seizures, and hearing loss, among others. Brain imaging may show cerebellar white matter abnormalities and/or bilateral thalamic lesions. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
4 |
Mitochondrial NeuroGastroIntestinal Encephalomyopathy (MNGIE) syndrome is characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
A rare, genetic, syndromic intellectual disability disorder characterized by congenital, external, nuclear ophthalmoplegia, lingua scrotalis, progressive chorioretinal sclerosis and intellectual disability. Bilateral ptosis, bilateral facial weakness, Parinaud's syndrome, convergence paresis and myopia may be associated. There have been no further descriptions in the literature since 1975. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
Progressive external ophthalmoplegia-myopathy-emaciation syndrome is a rare mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with generalized muscle wasting, profound emaciation, respiratory failure, spinal deformity and facial muscle weakness (manifesting with ptosis, dysphonia, dysphagia and nasal speech). Intellectual disability, gastrointestinal symptoms (e.g. nausea, abdominal fullness, and loss of appetite), dilated cardiomyopathy and renal colic have also been reported. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
4 |
A rare, genetic, non-dystrophic myopathy disease characterized by childhood-onset severe external ophthalmoplegia, typically without ptosis, associated with mild, very slowly progressive muscular weakness and atrophy, involving the facial, neck flexor and limb (upper > lower, proximal > distal) muscles. Muscle biopsy shows type 1 fiber uniformity, absent, or abnormally small, type 2A fibers, increased variability of fiber size, internalized nuclei and/or fatty infiltration. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
5 |
A rare genetic, neuro-ophthalmological disease characterized by progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse symmetric ophthalmoparesis. Additional signs may include skeletal muscle weakness, cataracts, hearing loss, sensory axonal neuropathy, ataxia, parkinsonism, cardiomyopathy, hypogonadism and depression. It is usually less severe than autosomal recessive form. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
A rare genetic, neuro-ophthalmological disease characterized by progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalized skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form. |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
Structure of extraocular muscle of left eye (body structure) |
Is a |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
|
Structure of extraocular muscle of right eye (body structure) |
Is a |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
|
Extraocular myositis |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Ocular muscle balance normal (finding) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
3 |
Autosomal dominant progressive external ophthalmoplegia type 4 (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Autosomal dominant progressive external ophthalmoplegia type 1 (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Autosomal dominant progressive external ophthalmoplegia type 5 |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Autosomal dominant progressive external ophthalmoplegia type 3 (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Chemodenervation of extraocular muscle |
Procedure site - Indirect (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Infiltrative extraocular myopathy (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Adhesion of extraocular muscle (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Disorder of orbital pulley (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Myopathy of extraocular muscle due to disorder of blood vessel (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |
Congenital multi-minicore disease with external ophthalmoplegia (disorder) |
Finding site |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
2 |
Injection into extraocular muscle (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of extraocular muscle |
Inferred relationship |
Some |
1 |