Laryngeal dystonia

Symptom Information:

Symptom ID: HPO:0012049
Synonyms:
Spasmodic dysphonia [HPO:0012049]
Laryngeal dystonia [OMIM:Laryngeal dystonia]
Spasmodic dysphonia [OMIM:Spasmodic dysphonia]
Dysphonia, spasmodic [OMIM:Dysphonia, spasmodic]
Spasmodic dysphonia [MedDRA:10067672]
Quality:
Cross references:
OMIM: "Laryngeal dystonia" [OMIM:Laryngeal dystonia]
OMIM: "Spasmodic dysphonia" [OMIM:Spasmodic dysphonia]
OMIM: "Dysphonia, spasmodic" [OMIM:Dysphonia, spasmodic]
Is a (Direct Parents):
HPO         Focal dystonia
HPO         Dysphonia
MedDRA Upper respiratory tract signs and symptoms
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 higher mental function(HPO:0011446)
                Neurological speech impairment(HPO:0002167)
                   Dysphonia(HPO:0001618)
                      Laryngeal dystonia(HPO:0012049)
             Abnormality of movement(HPO:0100022)
                Dystonia(HPO:0001332)
                   Focal dystonia(HPO:0004373)
                      Laryngeal dystonia(HPO:0012049)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of the upper respiratory tract(HPO:0002087)
                Abnormality of the larynx(HPO:0001600)
                   Abnormality of the voice(HPO:0001608)
                      Dysphonia(HPO:0001618)
                         Laryngeal dystonia(HPO:0012049)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Respiratory disorders NEC(MedDRA:10038716)
       Upper respiratory tract signs and symptoms(MedDRA:10046313)
          Laryngeal dystonia(HPO:0012049)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant focal dystonia, DYT25 (Orphanet:329466)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Dystonia 16 (Orphanet:210571)
Neuroferritinopathy (Orphanet:157846)
Primary dystonia, DYT21 type (Orphanet:306734)
Primary dystonia, DYT6 type (Orphanet:98806)
Spinocerebellar ataxia type 20 (Orphanet:101110)