Fasciculations

Symptom Information:

Symptom ID: HPO:0002380
Synonyms:
Fasciculation [HPO:0002380]
Muscle fasciculation [HPO:0002380]
Muscle fasciculation [Orphanet:43270]
Muscle fasciculation (finding) [Orphanet:43270]
Muscle twitch (finding) [Orphanet:43270]
Muscle twitch [Orphanet:43270]
Muscular fasciculation [Orphanet:43270]
Fasciculation [OMIM:Fasciculation]
Fasciculations [OMIM:Fasciculations]
Myoclonus/fasciculations [Orphanet:43270]
Muscle twitching [Orphanet:43270]
Muscle contractions involuntary [MedDRA:10028293]
Contraction skeletal muscle [MedDRA:10028293]
Fasciculation [MedDRA:10028293]
Fasciculation skeletal muscle [MedDRA:10028293]
Fibrillation skeletal muscle [MedDRA:10028293]
Muscle fasciculation [MedDRA:10028293]
Muscle fibrillation [MedDRA:10028293]
Muscle twitching [MedDRA:10028347]
Muscle twitch [MedDRA:10028347]
Twitch skeletal muscle [MedDRA:10028347]
Twitches [MedDRA:10028347]
Twitching [MedDRA:10028347]
Twitching cervical [MedDRA:10028347]
Twitching facial [MedDRA:10028347]
Twitching flexor [MedDRA:10028347]
Twitching masticatory [MedDRA:10028347]
Twitching of limbs [MedDRA:10028347]
Twitching of neck and face [MedDRA:10028347]
Fasciculations (after long disease duration) [OMIM:Fasciculations (after long disease duration)]
Fasciculations (in some patients) [OMIM:Fasciculations (in some patients)]
Fasciculations (less common) [OMIM:Fasciculations (less common)]
Quality:
Cross references:
Orphanet:43270 "Myoclonus/fasciculations" [Orphanet:43270]
OMIM: "Fasciculation" [OMIM:Fasciculation]
OMIM: "Fasciculations" [OMIM:Fasciculations]
OMIM: "Fasciculations (after long disease duration)" [OMIM:Fasciculations (after long disease duration)]
OMIM: "Fasciculations (in some patients)" [OMIM:Fasciculations (in some patients)]
OMIM: "Fasciculations (less common)" [OMIM:Fasciculations (less common)]
UMLS:C0015644 "Fasciculation" [HPO:0002380]
UMLS:C0231530 "Muscle twitch" [Orphanet:43270]
UMLS:C0015644 "Muscular fasciculation" [Orphanet:43270]
Is a (Direct Parents):
Orphanet Abnormality of movement
Orphanet Myoclonus
MedDRA Neuromuscular disorders NEC
HPO         Involuntary movements
MedDRA Muscle related signs and symptoms NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Involuntary movements(HPO:0004305)
                   Fasciculations(HPO:0002380)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Involuntary movements(HPO:0004305)
                Fasciculations(HPO:0002380)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neuromuscular disorders(MedDRA:10029317)
       Neuromuscular disorders NEC(MedDRA:10029318)
          Fasciculations(HPO:0002380)
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Muscle disorders(MedDRA:10028302)
       Muscle related signs and symptoms NEC(MedDRA:10028326)
          Fasciculations(HPO:0002380)
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 1 (OMIM:105400)
AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA (OMIM:613954)
AMYOTROPHIC LATERAL SCLEROSIS 17 (OMIM:614696)
AMYOTROPHIC LATERAL SCLEROSIS 18 (OMIM:614808)
AMYOTROPHIC LATERAL SCLEROSIS 5 (OMIM:602099)
AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA (OMIM:608030)
AMYOTROPHIC LATERAL SCLEROSIS 8 (OMIM:608627)
ATAXIA WITH FASCICULATIONS (OMIM:108700)
Adult-onset autosomal recessive cerebellar ataxia (Orphanet:284289)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Adult-onset proximal spinal muscular atrophy, autosomal dominant (Orphanet:209335)
Amyotrophic lateral sclerosis (Orphanet:803)
Autosomal dominant Charcot-Marie-Tooth disease type 2F (Orphanet:99940)
Autosomal dominant Charcot-Marie-Tooth disease type 2P (Orphanet:300319)
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal recessive axonal neuropathy with neuromyotonia (Orphanet:324442)
Autosomal recessive cerebellar ataxia - saccadic intrusion (Orphanet:95434)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
Erythrokeratodermia - ataxia (Orphanet:1955)
Fabry disease (Orphanet:324)
Hereditary motor and sensory neuropathy, Okinawa type (Orphanet:90117)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
Kennedy disease (Orphanet:481)
Lower motor neuron syndrome with late-adult onset (Orphanet:276435)
MELAS (Orphanet:550)
Monomelic amyotrophy (Orphanet:65684)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID (OMIM:615575)
Neutral lipid storage myopathy (Orphanet:98908)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1A (OMIM:607596)
Pontocerebellar hypoplasia type 1 (Orphanet:2254)
SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE (OMIM:611302)
SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE (OMIM:271200)
SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY (OMIM:183050)
Sandhoff disease (Orphanet:796)
Sandhoff disease, adult form (Orphanet:309169)
Sandhoff disease, infantile form (Orphanet:309155)
Sandhoff disease, juvenile form (Orphanet:309162)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
Spinocerebellar ataxia type 2 (Orphanet:98756)
Spinocerebellar ataxia type 3 (Orphanet:98757)
Spinocerebellar ataxia type 36 (Orphanet:276198)