Fasciculations
Symptom Information:
Symptom ID: | HPO:0002380 | ||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||
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) Involuntary movements(HPO:0004305) Fasciculations(HPO:0002380) 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) 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) |
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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) |