Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandOcular Motility Disorders (D015835)
Parent Node:
expandParalysis (D010243)
..Starting node
..expandOphthalmoplegia (D009886)

       Child Nodes:
........expandAdenine Nucleotide Translocator Deficiency (C566309)
........expandCANOMAD syndrome (C537980)
........expandExternal Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation (C566509)
........expandFibrosis Of Extraocular Muscles, Congenital, 2 (C566587)
........expandHamano Tsukamoto syndrome (C535625)
........expandInclusion Body Myopathy 3, Autosomal Dominant (C565311)
........expandInclusion body myopathy, autosomal dominant (C538330)
........expandMinicore Myopathy with External Ophthalmoplegia (C564969)
........expandMotor Neuron Disease with Dementia and Ophthalmoplegia (C563954)
........expandOcular Myopathy with Curare Sensitivity (C564937)
........expandOculomelic amyoplasia (C537737)
........expandOculootoradial syndrome (C535544)
........expandOphthalmoplegia Totalis with Ptosis and Miosis (C564927)
........expandOphthalmoplegia, Chronic Progressive External (D017246) Child7
........expandOphthalmoplegia, External, and Myopia (C564087)
........expandOphthalmoplegia, Familial Static (C563500)
........expandOphthalmoplegia, Familial Total, with Iris Transillumination (C563499)
........expandOphthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency (C563498)
........expandOphthalmoplegic Migraine (D060486)
........expandOphthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria (C564925)
........expandOptic Atrophy, Deafness, Ophthalmoplegia, and Myopathy (C565117)
........expandProgressive External Ophthalmoplegia With Hypogonadism (C563576)
........expandProgressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 (C563575)
........expandProgressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive (C564926)
........expandSchimke X-linked mental retardation syndrome (C536630)
........expandSensory ataxic neuropathy, dysarthria, and ophthalmoparesis (C537583)
........expandSupranuclear Palsy, Progressive (D013494) Child5
........expandTreft Sanborn Carey syndrome (C536544)
........expandWieacker syndrome (C536703)



 Sister Nodes: 
..expandFacial Paralysis (D005158) Child6
..expandGastroparesis (D018589)
..expandHemiplegia (D006429) Child1
..expandOphthalmoplegia (D009886) Child41
..expandParaplegia (D010264) Child14
..expandPseudobulbar Palsy (D020828) Child1
..expandQuadriplegia (D011782) Child4
..expandRespiratory Paralysis (D012133)
..expandVocal Cord Paralysis (D014826) Child6
..expandWells Jankovic syndrome (C536692)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:8252
Name:Ophthalmoplegia
Definition:Paralysis of one or more of the ocular muscles due to disorders of the eye muscles, neuromuscular junction, supporting soft tissue, tendons, or innervation to the muscles.
Alternative IDs:
ParentIDs:MESH:D010243|MESH:D015835
TreeNumbers:C10.292.562.750 |C10.597.622.447 |C11.590.472 |C23.888.592.636.447
Synonyms:External Ophthalmoplegia |External Ophthalmoplegias |Internal Ophthalmoplegia |Internal Ophthalmoplegias |Oculomotor Paralysis |Ophthalmopareses |Ophthalmoparesis |Ophthalmoplegia, External |Ophthalmoplegia, Internal |Ophthalmoplegias |Ophthalmoplegias, External |O
Slim Mappings:Eye disease|Nervous system disease|Signs and symptoms
Reference: MedGen: D009886
MeSH: D009886
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants