Muscle cramps

Symptom Information:

Symptom ID: HPO:0003394
Synonyms:
Muscle cramp [Orphanet:44200]
Cramp (finding) [Orphanet:44200]
Cramps [HPO:0003394]
Muscle Cramp [Orphanet:44200]
Muscle cramps [OMIM:Muscle cramps]
Contractures/cramps/trismus/tetania/claudication/opisthotonos [Orphanet:44200]
Muscle cramps [Orphanet:44200]
Muscle spasms [MedDRA:10028334]
Cramp [MedDRA:10028334]
Cramp in hand [MedDRA:10028334]
Cramp in legs thighs [MedDRA:10028334]
Cramp legs [MedDRA:10028334]
Cramp muscle [MedDRA:10028334]
Cramp of limb [MedDRA:10028334]
Cramps [MedDRA:10028334]
Cramps calf [MedDRA:10028334]
Cramps in legs [MedDRA:10028334]
Cramps in the calves [MedDRA:10028334]
Cramps leg [MedDRA:10028334]
Cramps legs [MedDRA:10028334]
Cramps of lower body [MedDRA:10028334]
Cramps of lower extremities [MedDRA:10028334]
Foot cramps [MedDRA:10028334]
Generalized spasm [MedDRA:10028334]
Leg cramps [MedDRA:10028334]
Muscle cramp [MedDRA:10028334]
Muscle cramps [MedDRA:10028334]
Muscle cramps aggravated [MedDRA:10028334]
Muscle spasm [MedDRA:10028334]
Muscular spasm [MedDRA:10028334]
Neck cramps [MedDRA:10028334]
Night cramps [MedDRA:10028334]
Nocturnal leg muscle cramps [MedDRA:10028334]
Spasm generalised [MedDRA:10028334]
Spasm generalized [MedDRA:10028334]
Spasm muscle [MedDRA:10028334]
Spasm of muscle [MedDRA:10028334]
Spasms [MedDRA:10028334]
Tetanic spasm generalized [MedDRA:10028334]
Cervical spasm [MedDRA:10028334]
Finger cramps [MedDRA:10028334]
Systremma [MedDRA:10028334]
Spasmophilia [MedDRA:10028334]
Charley horse [MedDRA:10028334]
Back muscle spasms [MedDRA:10028334]
Generalised spasm [MedDRA:10028334]
Tetanic spasm generalised [MedDRA:10028334]
Cramps [OMIM:Cramps]
Leg cramps [OMIM:Leg cramps]
Muscle cramps (also seen in some heterozygotes) [OMIM:Muscle cramps (also seen in some heterozygotes)]
Muscle spasm [OMIM:Muscle spasm]
Muscles cramps [OMIM:Muscles cramps]
Muscle contracture [Orphanet:44200]
Contracture (morphologic abnormality) [Orphanet:44200]
Spasm (finding) [Orphanet:44200]
Muscle contracture (disorder) [Orphanet:44200]
Contracture [Orphanet:44200]
Spasm [Orphanet:44200]
Quality:
Cross references:
Orphanet:44200 "Contractures/cramps/trismus/tetania/claudication/opisthotonos" [Orphanet:44200]
OMIM: "Muscle cramps" [OMIM:Muscle cramps]
OMIM: "Cramps" [OMIM:Cramps]
OMIM: "Leg cramps" [OMIM:Leg cramps]
OMIM: "Muscle cramps (also seen in some heterozygotes)" [OMIM:Muscle cramps (also seen in some heterozygotes)]
OMIM: "Muscle spasm" [OMIM:Muscle spasm]
OMIM: "Muscles cramps" [OMIM:Muscles cramps]
UMLS:C0026821 "Cramps" [HPO:0003394]
UMLS:C0026821 "Muscle Cramp" [Orphanet:44200]
UMLS:C0009917 "Contracture" [Orphanet:44200]
UMLS:C0037763 "Spasm" [Orphanet:44200]
Is a (Direct Parents):
Orphanet Trismus
HPO         Abnormality of muscle physiology
Orphanet Muscle anomalies
MedDRA Muscle related signs and symptoms NEC
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)
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)