Dysphonia
Symptom Information:
Symptom ID: | HPO:0001618 | ||||||||||||||||||||||||
Synonyms: |
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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 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) 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) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Respiratory disorders NEC(MedDRA:10038716) Upper respiratory tract signs and symptoms(MedDRA:10046313) Dysphonia(HPO:0001618) |
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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) |