Dysphonia

Symptom Information:

Symptom ID: HPO:0001618
Synonyms:
Dysphonia [Orphanet:43490]
Dysphonia [OMIM:Dysphonia]
Elocution disorders/dysarthria/dysphonia [Orphanet:43490]
Dysphonia [MedDRA:10013952]
Distorted voice [MedDRA:10013952]
Disturbance in loudness [MedDRA:10013952]
Hoarse voice [MedDRA:10013952]
Hoarseness [MedDRA:10013952]
Hoarseness of voice [MedDRA:10013952]
Other voice disturbance [MedDRA:10013952]
Phonation difficulty [MedDRA:10013952]
Resonance disorder [MedDRA:10013952]
Vocal tone disorder [MedDRA:10013952]
Vocal volume disorder [MedDRA:10013952]
Voice alteration [MedDRA:10013952]
Voice disturbance [MedDRA:10013952]
Voice disturbance, unspecified [MedDRA:10013952]
Voice lowered [MedDRA:10013952]
Hypophonia [MedDRA:10013952]
Rhinolalia [MedDRA:10013952]
Hoarseness (53%) [OMIM:Hoarseness (53%)]
Communication disorder [Orphanet:43490]
Communications disorders [MedDRA:10010119]
Communication disorder [MedDRA:10061046]
Quality:
Cross references:
Orphanet:43490 "Elocution disorders/dysarthria/dysphonia" [Orphanet:43490]
OMIM: "Dysphonia" [OMIM:Dysphonia]
OMIM: "Hoarseness (53%)" [OMIM:Hoarseness (53%)]
UMLS:C1527344 "Dysphonia" [HPO:0001618]
UMLS:C1527344 "Dysphonia" [Orphanet:43490]
Is a (Direct Parents):
HPO         Abnormality of the voice
MedDRA Upper respiratory tract signs and symptoms
MedDRA Dysarthria
HPO         Neurological speech impairment
Orphanet Functional anomalies of the nervous system
MedDRA Communication disorders and disturbances
Orphanet Dysarthria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
       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)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Respiratory disorders NEC(MedDRA:10038716)
       Upper respiratory tract signs and symptoms(MedDRA:10046313)
          Dysphonia(HPO:0001618)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
Aceruloplasminemia (Orphanet:48818)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Autosomal dominant cervical dystonia (Orphanet:93962)
Autosomal dominant focal dystonia, DYT25 (Orphanet:329466)
Autosomal dominant focal dystonia, DYT7 type (Orphanet:93963)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE (OMIM:612406)
DYSTONIA 23 (OMIM:614860)
DYSTONIA WITH CEREBELLAR ATROPHY (OMIM:611694)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
HERNS syndrome (Orphanet:63261)
Hereditary motor and sensory neuropathy type 5 (Orphanet:64751)
LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY (OMIM:606183)
MELAS (Orphanet:550)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Neuroferritinopathy (Orphanet:157846)
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS (OMIM:614369)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Primary dystonia, DYT4 type (Orphanet:98805)
Primary dystonia, DYT6 type (Orphanet:98806)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)
Spinocerebellar ataxia type 20 (Orphanet:101110)
VACUOLAR NEUROMYOPATHY (OMIM:601846)
Wolfram syndrome (Orphanet:3463)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)