Ophthalmoparesis

Symptom Information:

Symptom ID: HPO:0000597
Synonyms:
Extraocular muscle palsy [HPO:0000597]
Extraocular muscle paralysis [HPO:0000597]
Oculomotor nerve palsy [Orphanet:5930]
Ophthalmoplegia (disorder) [Orphanet:5930]
Ophthalmoplegia [Orphanet:5930]
Ophthalmoparesis [Orphanet:5930]
Oculomotor Nerve Paralysis [Orphanet:5930]
Extraocular muscle palsy [OMIM:Extraocular muscle palsy]
Extraocular muscle paralysis [OMIM:Extraocular muscle paralysis]
Ophthalmoparesis [OMIM:Ophthalmoparesis]
Ophthalmoplegia/ophthalmoparesis/oculomotor palsy [Orphanet:5930]
IIIrd nerve paralysis [Orphanet:5930]
IIIrd nerve paralysis [MedDRA:10021283]
Cranial third nerve paralysis [MedDRA:10021283]
IIIrd nerve palsy [MedDRA:10021283]
Oculomotor nerve paralysis [MedDRA:10021283]
Oculomotor paralysis [MedDRA:10021283]
Paralysis oculomotor [MedDRA:10021283]
Third nerve paralysis [MedDRA:10021283]
Third or oculomotor nerve palsy, partial [MedDRA:10021283]
Third or oculomotor nerve palsy, total [MedDRA:10021283]
Ophthalmoplegia [MedDRA:10030875]
Exophthalmic ophthalmoplegia [MedDRA:10030875]
External ophthalmoplegia [MedDRA:10030875]
Extraocular palsy [MedDRA:10030875]
Eye muscle paralysis [MedDRA:10030875]
Internuclear ophthalmoplegia [MedDRA:10030875]
Muscle paralysis eye [MedDRA:10030875]
Ophthalmoplegia externa [MedDRA:10030875]
Ophthalmoplegia interna [MedDRA:10030875]
Ophthalmoplegia NOS [MedDRA:10030875]
Palsy extraocular [MedDRA:10030875]
Paralysis extraocular muscle (s) [MedDRA:10030875]
Total ophthalmoplegia [MedDRA:10030875]
Total or complete internal ophthalmoplegia [MedDRA:10030875]
Ophthalmoplegia (NOS) [MedDRA:10030875]
L'Hermitte syndrome [MedDRA:10030875]
MLF syndrome [MedDRA:10030875]
Medial longitudinal fasciculus syndrome [MedDRA:10030875]
External ophthalmoplegia (less common) [OMIM:External ophthalmoplegia (less common)]
External ophthalmoplegia (uncommon) [OMIM:External ophthalmoplegia (uncommon)]
Ophthalmoparesis (less common) [OMIM:Ophthalmoparesis (less common)]
Ophthalmoparesis (with longer disease duration) [OMIM:Ophthalmoparesis (with longer disease duration)]
Ophthalmoplegia (in 20%) [OMIM:Ophthalmoplegia (in 20%)]
Ophthalmoplegia (in some) [OMIM:Ophthalmoplegia (in some)]
Quality:
Cross references:
HPO:0000544 "External ophthalmoplegia" [Orphanet:5930]
HPO:0000602 "Ophthalmoplegia" [Orphanet:5930]
Orphanet:5930 "Ophthalmoplegia/ophthalmoparesis/oculomotor palsy" [Orphanet:5930]
OMIM: "Extraocular muscle palsy" [OMIM:Extraocular muscle palsy]
OMIM: "Extraocular muscle paralysis" [OMIM:Extraocular muscle paralysis]
OMIM: "Ophthalmoparesis" [OMIM:Ophthalmoparesis]
OMIM: "External ophthalmoplegia (less common)" [OMIM:External ophthalmoplegia (less common)]
OMIM: "External ophthalmoplegia (uncommon)" [OMIM:External ophthalmoplegia (uncommon)]
OMIM: "Ophthalmoparesis (less common)" [OMIM:Ophthalmoparesis (less common)]
OMIM: "Ophthalmoparesis (with longer disease duration)" [OMIM:Ophthalmoparesis (with longer disease duration)]
OMIM: "Ophthalmoplegia (in 20%)" [OMIM:Ophthalmoplegia (in 20%)]
OMIM: "Ophthalmoplegia (in some)" [OMIM:Ophthalmoplegia (in some)]
UMLS:C0751401 "Ophthalmoparesis" [HPO:0000597]
UMLS:C0029089 "Ophthalmoplegia" [Orphanet:5930]
UMLS:C0751401 "Ophthalmoparesis" [Orphanet:5930]
UMLS:C0028866 "Oculomotor Nerve Paralysis" [Orphanet:5930]
Is a (Direct Parents):
HPO         Abnormality of eye movement
MedDRA Ocular signs and symptoms NEC
Orphanet Abnormality of eye movement
MedDRA Ocular nerve and muscle disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of eye movement(HPO:0000496)
                Ophthalmoparesis(HPO:0000597)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders of the eye(MedDRA:10029301)
       Ocular signs and symptoms NEC(MedDRA:10030952)
          Ophthalmoparesis(HPO:0000597)
Eye disorders(MedDRA:10015919)
    Ocular neuromuscular disorders(MedDRA:10030061)
       Ocular nerve and muscle disorders(MedDRA:10030059)
          Ophthalmoparesis(HPO:0000597)
Database Frequency: 71 / 7739
Resource:

All diseases associated with this symptom:

Acetazolamide-responsive myotonia (Orphanet:99736)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Atypical progressive supranuclear palsy (Orphanet:99750)
Autosomal dominant cerebellar ataxia (Orphanet:99)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
Behr syndrome (Orphanet:1239)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Centronuclear myopathy (Orphanet:595)
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss (Orphanet:1171)
Christianson syndrome (Orphanet:85278)
Congenital myasthenic syndromes with glycosylation defect (Orphanet:353327)
Crigler-Najjar syndrome (Orphanet:205)
Crigler-Najjar syndrome type 1 (Orphanet:79234)
Deafness - small bowel diverticulosis - neuropathy (Orphanet:3217)
Duane anomaly - myopathy - scoliosis (Orphanet:50817)
Duane retraction syndrome (Orphanet:233)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1 (OMIM:158900)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Giant cell arteritis (Orphanet:397)
Horizontal gaze palsy with progressive scoliosis (Orphanet:2744)
Hyperkalemic periodic paralysis (Orphanet:682)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Kearns-Sayre syndrome (Orphanet:480)
Leigh syndrome (Orphanet:506)
Linear nevus sebaceus syndrome (Orphanet:2612)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA (OMIM:600333)
MYASTHENIC SYNDROME, CONGENITAL, 10 (OMIM:254300)
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL (OMIM:601462)
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL (OMIM:608930)
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL (OMIM:605809)
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:608931)
MYOPATHY, CENTRONUCLEAR, 1 (OMIM:160150)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION (OMIM:255310)
Macrostomia - preauricular tags - external ophthalmoplegia (Orphanet:83619)
Maternally-inherited cardiomyopathy and hearing loss (Orphanet:1349)
Maternally-inherited diabetes and deafness (Orphanet:225)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Moebius syndrome (Orphanet:570)
Myasthenia gravis (Orphanet:589)
Myotonia fluctuans (Orphanet:99734)
Myotonia permanens (Orphanet:99735)
Neuronal intranuclear inclusion disease (Orphanet:2289)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 (OMIM:259700)
Oculogastrointestinal muscular dystrophy (Orphanet:1876)
Oculopharyngeal muscular dystrophy (Orphanet:270)
Ophthalmoplegia - intellectual deficit - lingua scrotalis (Orphanet:2743)
Ophthalmoplegia - myalgia - tubular aggregates (Orphanet:2742)
Perrault Syndrome (Orphanet:2855)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Postsynaptic congenital myasthenic syndromes (Orphanet:98913)
Potassium-aggravated myotonia (Orphanet:612)
Presynaptic congenital myasthenic syndromes (Orphanet:98914)
Progressive supranuclear palsy - parkinsonism (Orphanet:240085)
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia (Orphanet:3390)
Retinitis pigmentosa (Orphanet:791)
Rhabdoid tumor (Orphanet:69077)
Spinocerebellar ataxia type 28 (Orphanet:101109)
Sporadic Leigh syndrome (Orphanet:255199)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Synaptic congenital myasthenic syndromes (Orphanet:98915)
Wolfram syndrome (Orphanet:3463)
X-linked centronuclear myopathy (Orphanet:596)