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:
expand
Muscular Diseases (D009135)
Parent Node:
expand
Neuromuscular Diseases (D009468)
Parent Node:
expand
Peripheral Nervous System Diseases (D010523)
..Starting node
..expand
Isaacs Syndrome (D020386)

       Child Nodes:



 Sister Nodes: 
..expandAccessory deep peroneal nerve (C536001)
..expandAcrodynia (D000170)
..expandAmyloid Neuropathies (D017772) Child3
..expandBrachial Plexus Neuropathies (D020516) Child4
..expandCataract ataxia deafness (C538283)
..expandComplex Regional Pain Syndromes (D020918) Child2
..expandCorpus callosum agenesis neuronopathy (C536446)
..expandDeafness, X-Linked 5 (C564472)
..expandDiabetic Neuropathies (D003929) Child2
..expandGiant Axonal Neuropathy (D056768) Child1
..expandGuillain-Barre Syndrome (D020275) Child1
..expandHand-Arm Vibration Syndrome (D053421)
..expandHypertrophic Neuropathy And Cataract (C565490)
..expandInherited Peripheral Neuropathy (C548028)
..expandIsaacs Syndrome (D020386)
..expandMononeuropathies (D020422) Child15
..expandNavajo neurohepatopathy (C538344) Child1
..expandNerve Compression Syndromes (D009408) Child13
..expandNeuralgia (D009437) Child6
..expandNeuritis (D009443) Child3
..expandNeurofibromatosis 1 (D009456) Child1
..expandNEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC (OMIM:613376)
..expandNeuropathy, Painful (C564945)
..expandNeuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine (C563516)
..expandOptic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
..expandPain Insensitivity, Congenital (D000699) Child2
..expandPeripheral Nerve Injuries (D059348)
..expandPeripheral Nervous System Neoplasms (D010524) Child25
..expandPeripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain (C564894)
..expandPolyneuropathies (D011115) Child200
..expandRadiculopathy (D011843)
..expandSacral plexopathy (C537224)
..expandSpinocerebellar Ataxia With Rigidity And Peripheral Neuropathy (C566669)
..expandTarlov Cysts (D052958)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5920
Name:Isaacs Syndrome
Definition:A rare neuromuscular disorder with onset usually in late childhood or early adulthood, characterized by intermittent or continuous widespread involuntary muscle contractions; FASCICULATION; hyporeflexia; MUSCLE CRAMP; MUSCLE WEAKNESS; HYPERHIDROSIS; TACHYCARDIA; and MYOKYMIA. Involvement of pharyngeal or laryngeal muscles may interfere with speech and breathing. The continuous motor activity persists during sleep and general anesthesia (distinguishing this condition from STIFF-PERSON SYNDROME). Familial and acquired (primarily autoimmune) forms have been reported. (From Ann NY Acad Sci 1998 May 13;841:482-496; Adams et al., Principles of Neurology, 6th ed, p1491)
Alternative IDs:
ParentIDs:MESH:D009135|MESH:D009468|MESH:D010523
TreeNumbers:C05.651.392 |C10.668.402 |C10.668.829.425
Synonyms:Acquired Neuromyotonia |Continuous Muscle Activity Syndrome |Continuous Myokymia |Continuous Myokymias |Gamstorp Wohlfart Syndrome |Gamstorp-Wohlfart Syndrome |Gamstorp-Wohlfart Syndromes |Isaacs Mertens Syndrome |Isaacs-Mertens Syndrome |Isaacs Pseudomyotonia Sy
Slim Mappings:Musculoskeletal disease|Nervous system disease
Reference: MedGen: D020386
MeSH: D020386
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants