External ophthalmoplegia

Symptom Information:

Symptom ID: HPO:0000544
Synonyms:
Ophthalmoplegia externa [HPO:0000544]
Oculomotor nerve palsy [Orphanet:5930]
Ophthalmoplegia (disorder) [Orphanet:5930]
Ophthalmoplegia [Orphanet:5930]
Ophthalmoparesis [Orphanet:5930]
Oculomotor Nerve Paralysis [Orphanet:5930]
External ophthalmoplegia [OMIM:External 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:0000597 "Ophthalmoparesis" [Orphanet:5930]
HPO:0000602 "Ophthalmoplegia" [Orphanet:5930]
Orphanet:5930 "Ophthalmoplegia/ophthalmoparesis/oculomotor palsy" [Orphanet:5930]
OMIM: "External ophthalmoplegia" [OMIM:External 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" [Orphanet:5930]
UMLS:C0751401 "Ophthalmoparesis" [Orphanet:5930]
UMLS:C0028866 "Oculomotor Nerve Paralysis" [Orphanet:5930]
Is a (Direct Parents):
HPO         Ophthalmoplegia
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)
                   Ophthalmoplegia(HPO:0000602)
                      External ophthalmoplegia(HPO:0000544)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders of the eye(MedDRA:10029301)
       Ocular signs and symptoms NEC(MedDRA:10030952)
          External ophthalmoplegia(HPO:0000544)
Eye disorders(MedDRA:10015919)
    Ocular neuromuscular disorders(MedDRA:10030061)
       Ocular nerve and muscle disorders(MedDRA:10030059)
          External ophthalmoplegia(HPO:0000544)
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant centronuclear myopathy (Orphanet:169189)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Biotin-responsive basal ganglia disease (Orphanet:65284)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital myasthenic syndromes (Orphanet:590)
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1 (OMIM:158900)
Facioscapulohumeral dystrophy (Orphanet:269)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
IVIC syndrome (Orphanet:2307)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Intellectual deficit, X-linked, Schimke type (Orphanet:85285)
Kearns-Sayre syndrome (Orphanet:480)
Leigh syndrome (Orphanet:506)
Linear nevus sebaceus syndrome (Orphanet:2612)
MELAS (Orphanet:550)
MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS (OMIM:254190)
MYASTHENIC SYNDROME, CONGENITAL, 10 (OMIM:254300)
MYASTHENIC SYNDROME, CONGENITAL, 16 (OMIM:614198)
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 renal tubulopathy (Orphanet:255235)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION (OMIM:165098)
Oculogastrointestinal muscular dystrophy (Orphanet:1876)
Oculopharyngodistal myopathy (Orphanet:98897)
Perrault Syndrome 5 (OMIM:616138)
Riboflavin transporter deficiency (Orphanet:97229)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 (OMIM:615768)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Spinocerebellar ataxia type 28 (Orphanet:101109)
Spinocerebellar ataxia type 3 (Orphanet:98757)
Sporadic Leigh syndrome (Orphanet:255199)
Thiamine-responsive encephalopathy (Orphanet:199348)
Tubular aggregate myopathy (Orphanet:2593)
Wolfram syndrome (Orphanet:3463)
X-linked centronuclear myopathy (Orphanet:596)