Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandCranial Nerve Diseases (D003389)
Parent Node:
expandDemyelinating Diseases (D003711)
Parent Node:
expandMigraine Disorders (D008881)
Parent Node:
expandOphthalmoplegia (D009886)
..Starting node
..expandOphthalmoplegic Migraine (D060486)

       Child Nodes:



 Sister 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)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:8260
Name:Ophthalmoplegic Migraine
Definition:Childhood-onset of recurrent headaches with an oculomotor cranial nerve palsy. Typically, ABDUCENS NERVE; OCULOMOTOR NERVE; and TROCHLEAR NERVE are involved with DIPLOPIA and BLEPHAROPTOSIS.
Alternative IDs:
ParentIDs:MESH:D003389|MESH:D003711|MESH:D008881|MESH:D009886
TreeNumbers:C10.228.140.546.399.750.725 |C10.292.562.750.375 |C10.292.675 |C10.314.687 |C10.597.622.447.600 |C11.590.472.375 |C23.888.592.636.447.600
Synonyms:Migraine, Ophthalmoplegic |Migraines, Ophthalmoplegic |Migraine Syndrome, Ophthalmoplegic |Migraine Syndromes, Ophthalmoplegic |Ophthalmoplegic Migraines |Ophthalmoplegic Migraine Syndrome |Ophthalmoplegic Migraine Syndromes |Syndrome, Ophthalmoplegic Migraine |
Slim Mappings:Eye disease|Nervous system disease|Signs and symptoms
Reference: MedGen: D060486
MeSH: D060486
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants