Muscle cramps
Symptom Information:
Symptom ID: | HPO:0003394 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle cramps(HPO:0003394) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle related signs and symptoms NEC(MedDRA:10028326) Muscle cramps(HPO:0003394) |
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Database Frequency: | 106 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADENOSINE MONOPHOSPHATE DEAMINASE 1 | (OMIM:102770) |
AMYOTROPHIC LATERAL SCLEROSIS 1 | (OMIM:105400) |
AMYOTROPHIC LATERAL SCLEROSIS 8 | (OMIM:608627) |
Acanthosis nigricans - Insulin resistance - muscle cramps - acral enlargement | (Orphanet:90301) |
Acetazolamide-responsive myotonia | (Orphanet:99736) |
Alopecia-intellectual deficit syndrome | (Orphanet:2850) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Amyotrophic lateral sclerosis | (Orphanet:803) |
Amyotrophic lateral sclerosis-parkinsonism-dementia complex | (Orphanet:90020) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Autosomal dominant Charcot-Marie-Tooth disease type 2F | (Orphanet:99940) |
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures | (Orphanet:73229) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A | (Orphanet:100043) |
Autosomal dominant limb-girdle muscular dystrophy type 1C | (Orphanet:265) |
Autosomal recessive axonal neuropathy with neuromyotonia | (Orphanet:324442) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2S | (Orphanet:369840) |
Autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia | (Orphanet:30924) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Bartter syndrome | (Orphanet:112) |
Bartter syndrome with hypocalcemia | (Orphanet:263417) |
Becker muscular dystrophy | (Orphanet:98895) |
Brody myopathy | (Orphanet:53347) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CHILD syndrome | (Orphanet:139) |
Canavan disease | (Orphanet:141) |
Carnitine palmitoyl transferase II deficiency | (Orphanet:157) |
Carnitine palmitoyl transferase II deficiency, myopathic form | (Orphanet:228302) |
Complete androgen insensitivity syndrome | (Orphanet:99429) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Congenital myasthenic syndromes with glycosylation defect | (Orphanet:353327) |
Cutis laxa-Marfanoid syndrome | (Orphanet:171719) |
De Barsy syndrome | (Orphanet:2962) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Dracunculiasis | (Orphanet:231) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Fabry disease | (Orphanet:324) |
Gaucher disease type 2 | (Orphanet:77260) |
Gitelman syndrome | (Orphanet:358) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency | (Orphanet:284426) |
Glycogen storage disease due to lactate dehydrogenase deficiency | (Orphanet:2364) |
Glycogen storage disease due to phosphoglucomutase deficiency | (Orphanet:711) |
Glycogen storage disease due to phosphoglycerate mutase deficiency | (Orphanet:97234) |
HYPOCALCEMIA, AUTOSOMAL DOMINANT 2 | (OMIM:615361) |
HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY | (OMIM:241150) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Hypoparathyroidism - deafness - renal disease | (Orphanet:2237) |
Ichthyosis hystrix of Curth-Macklin | (Orphanet:79503) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Juvenile dermatomyositis | (Orphanet:93672) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
Kennedy disease | (Orphanet:481) |
Kindler syndrome | (Orphanet:2908) |
Leber plus disease | (Orphanet:99718) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
MELAS | (Orphanet:550) |
MUSCLE CRAMPS, FAMILIAL | (OMIM:158400) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYASTHENIC SYNDROME, CONGENITAL, 12 | (OMIM:610542) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
MYOPATHY, CENTRONUCLEAR, 3 | (OMIM:614408) |
MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES | (OMIM:616231) |
MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS | (OMIM:160990) |
MYXEDEMA | (OMIM:255900) |
Majeed syndrome | (Orphanet:77297) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Myotonia fluctuans | (Orphanet:99734) |
Myotonia permanens | (Orphanet:99735) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID | (OMIM:615575) |
Neu-Laxova syndrome | (Orphanet:2671) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Oral submucous fibrosis | (Orphanet:357154) |
PARKINSON DISEASE 17 | (OMIM:614203) |
PEHO syndrome | (Orphanet:2836) |
Porphyria | (Orphanet:738) |
Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
Potassium-aggravated myotonia | (Orphanet:612) |
Primary orthostatic tremor | (Orphanet:238606) |
Proximal spinal muscular atrophy type 3 | (Orphanet:83419) |
Pseudohypoaldosteronism type 2 | (Orphanet:757) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Sialidosis type 2 | (Orphanet:87876) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | (Orphanet:206546) |
Thoracic outlet syndrome | (Orphanet:97330) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Tubular aggregate myopathy | (Orphanet:2593) |
Williams syndrome | (Orphanet:904) |