Ophthalmoplegia

Symptom Information:

Symptom ID: HPO:0000602
Synonyms:
Oculomotor nerve palsy [Orphanet:5930]
Ophthalmoplegia (disorder) [Orphanet:5930]
Ophthalmoplegia [Orphanet:5930]
Ophthalmoparesis [Orphanet:5930]
Oculomotor Nerve Paralysis [Orphanet:5930]
Ophthalmoplegia [OMIM:Ophthalmoplegia]
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:0000597 "Ophthalmoparesis" [Orphanet:5930]
Orphanet:5930 "Ophthalmoplegia/ophthalmoparesis/oculomotor palsy" [Orphanet:5930]
OMIM: "Ophthalmoplegia" [OMIM:Ophthalmoplegia]
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:C0029089 "Ophthalmoplegia" [HPO:0000602]
UMLS:C0029089 "Ophthalmoplegia" [Orphanet:5930]
UMLS:C0751401 "Ophthalmoparesis" [Orphanet:5930]
UMLS:C0028866 "Oculomotor Nerve Paralysis" [Orphanet:5930]
Is a (Direct Parents):
MedDRA Ocular signs and symptoms NEC
HPO         Ophthalmoparesis
MedDRA Ocular nerve and muscle disorders
Orphanet Abnormality of eye movement
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)
                   Ophthalmoplegia(HPO:0000602)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders of the eye(MedDRA:10029301)
       Ocular signs and symptoms NEC(MedDRA:10030952)
          Ophthalmoplegia(HPO:0000602)
Eye disorders(MedDRA:10015919)
    Ocular neuromuscular disorders(MedDRA:10030061)
       Ocular nerve and muscle disorders(MedDRA:10030059)
          Ophthalmoplegia(HPO:0000602)
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
AL amyloidosis (Orphanet:85443)
Aarskog-Scott syndrome (Orphanet:915)
Alström syndrome (Orphanet:64)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
Charcot-Marie-Tooth disease type 4B3 (Orphanet:363981)
Christianson syndrome (Orphanet:85278)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Combined oxidative phosphorylation defect type 7 (Orphanet:254930)
Congenital fiber-type disproportion myopathy (Orphanet:2020)
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)
Gordon syndrome (Orphanet:376)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Isolated succinate-CoQ reductase deficiency (Orphanet:3208)
Kearns-Sayre syndrome (Orphanet:480)
Leber plus disease (Orphanet:99718)
Leigh syndrome (Orphanet:506)
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate (Orphanet:314051)
Linear nevus sebaceus syndrome (Orphanet:2612)
MELAS (Orphanet:550)
MYASTHENIC SYNDROME, CONGENITAL, 10 (OMIM:254300)
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL (OMIM:601462)
MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL (OMIM:616313)
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL (OMIM:616322)
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL (OMIM:616324)
MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616325)
MYOPATHY, CENTRONUCLEAR, 5 (OMIM:615959)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION (OMIM:255310)
Maternally-inherited diabetes and deafness (Orphanet:225)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
NEMALINE MYOPATHY 10 (OMIM:616165)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS (OMIM:258400)
OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA (OMIM:311000)
OPHTHALMOPLEGIA, FAMILIAL STATIC (OMIM:165000)
OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA (OMIM:258470)
Oculogastrointestinal muscular dystrophy (Orphanet:1876)
Perrault Syndrome 5 (OMIM:616138)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary localized amyloidosis (Orphanet:314709)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Spinocerebellar ataxia type 2 (Orphanet:98756)
Spinocerebellar ataxia type 28 (Orphanet:101109)
Sporadic Leigh syndrome (Orphanet:255199)
WERNICKE-KORSAKOFF SYNDROME (OMIM:277730)
Wolfram syndrome (Orphanet:3463)