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Ontology Browser

Term:
familial periodic paralysis (DOID:1029)
Annotations: Rat: (16) Mouse: (17) Human: (18) Chinchilla: (14) Bonobo: (15) Dog: (16) Squirrel: (14) Pig: (14)
Parent Terms Term With Siblings Child Terms
acrodermatitis enteropathica  
Arthrogryposis +   
atransferrinemia  
atrophic muscular disease +   
autosomal dominant hypocalcemia +   
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Carey-Fineman-Ziter syndrome  
chronic fatigue syndrome  
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Contracture +   
Craniomandibular Disorders +   
diaphragm disease +   
Dimauro Disease  
Early-Onset Myopathy with Fatal Cardiomyopathy  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
eosinophilia-myalgia syndrome  
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
Familial Hypophosphatemia +   
familial periodic paralysis +   
A heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481)
fibromyalgia +   
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
hemochromatosis +   
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hypermanganesemia with dystonia +   
Hypertrophia Musculorum Vera 
Hyperzincemia and Hypercalprotectinemia 
Hyperzincemia with Functional Zinc Depletion 
hypophosphatasia +   
Idiopathic Copper Toxicosis 
Internal Anal Sphincter Myopathy 
Kocher-Debre-Semelaigne Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Menkes disease +   
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
molybdenum cofactor deficiency +   
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
Myopathic Carnitine Deficiency 
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
myositis +   
myostatin-related muscle hypertrophy  
myotonic disease +   
Myotoxicity 
neutral lipid storage disease +   
occipital horn syndrome  
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
primary hypomagnesemia +   
Proximal Myopathy with Focal Depletion of Mitochondria 
pseudohypoparathyroidism +   
Rhabdomyolysis +   
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Treft Sanborn Carey Syndrome 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Uruguay faciocardiomusculoskeletal syndrome  
Vacuolar Myopathy  
very long chain acyl-CoA dehydrogenase deficiency  
Wilson disease +   
Zinc, Elevated Plasma 

Synonyms
Exact Synonyms: familial periodic paralyses ;   normokalemic periodic paralyses ;   normokalemic periodic paralysis
Primary IDs: MESH:D010245
Xrefs: GARD:6422 ;   NCI:C84709
Definition Sources: MESH:D010245

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