Tongue fasciculations

Symptom Information:

Symptom ID: HPO:0001308
Synonyms:
Tongue fasciculation [HPO:0001308]
Tongue fasciculations/fibrillations [HPO:0001308]
Tongue fasciculations [OMIM:Tongue fasciculations]
Tongue fasciculations/fibrillations [OMIM:Tongue fasciculations/fibrillations]
Tongue fasciculation/fibrillation [OMIM:Tongue fasciculation/fibrillation]
Tongue fasciculations (1 patient) [OMIM:Tongue fasciculations (1 patient)]
Quality:
Cross references:
OMIM: "Tongue fasciculations" [OMIM:Tongue fasciculations]
OMIM: "Tongue fasciculations/fibrillations" [OMIM:Tongue fasciculations/fibrillations]
OMIM: "Tongue fasciculation/fibrillation" [OMIM:Tongue fasciculation/fibrillation]
OMIM: "Tongue fasciculations (1 patient)" [OMIM:Tongue fasciculations (1 patient)]
Is a (Direct Parents):
HPO         Abnormality of the tongue
HPO         Fasciculations
HPO         Muscle fibrillation
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)
                Muscle fibrillation(HPO:0010546)
                   Tongue fasciculations(HPO:0001308)
                Involuntary movements(HPO:0004305)
                   Fasciculations(HPO:0002380)
                      Tongue fasciculations(HPO:0001308)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Involuntary movements(HPO:0004305)
                Fasciculations(HPO:0002380)
                   Tongue fasciculations(HPO:0001308)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the tongue(HPO:0000157)
                         Tongue fasciculations(HPO:0001308)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 12 (OMIM:613435)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
BROWN-VIALETTO-VAN LAERE SYNDROME 2 (OMIM:614707)
Charcot-Marie-Tooth disease type 4C (Orphanet:99949)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B (OMIM:614678)
Proximal spinal muscular atrophy (Orphanet:70)
Proximal spinal muscular atrophy type 1 (Orphanet:83330)
Proximal spinal muscular atrophy type 2 (Orphanet:83418)
Proximal spinal muscular atrophy type 3 (Orphanet:83419)
Proximal spinal muscular atrophy type 4 (Orphanet:83420)
Riboflavin transporter deficiency (Orphanet:97229)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
Spinocerebellar ataxia type 36 (Orphanet:276198)
Spondyloepiphyseal dysplasia, Reardon type (Orphanet:163662)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)