Hoarse voice
Symptom Information:
Symptom ID: | HPO:0001609 | ||||||
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 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) Hoarse voice(HPO:0001609) MedDRA: |
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Database Frequency: | 34 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acromicric dysplasia | (Orphanet:969) |
Aspartylglucosaminuria | (Orphanet:93) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
Congenital laryngeal web | (Orphanet:2374) |
Costello syndrome | (Orphanet:3071) |
Diastrophic dwarfism | (Orphanet:628) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
Hereditary sensory and autonomic neuropathy type 1B | (Orphanet:139564) |
Isolated thyrotropin-releasing hormone deficiency | (Orphanet:238670) |
Keipert syndrome | (Orphanet:2662) |
LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY | (OMIM:606183) |
LARYNGEAL ADDUCTOR PARALYSIS | (OMIM:150270) |
Lipoid proteinosis | (Orphanet:530) |
MYXEDEMA | (OMIM:255900) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
PACHYONYCHIA CONGENITA 2 | (OMIM:167210) |
PARAGANGLIOMAS 1 | (OMIM:168000) |
PARAGANGLIOMAS 2 | (OMIM:601650) |
PARAGANGLIOMAS 3 | (OMIM:605373) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
Rudiger syndrome | (Orphanet:3118) |
Smith-Magenis syndrome | (Orphanet:819) |
Spondyloepimetaphyseal dysplasia, aggrecan type | (Orphanet:171866) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Tracheobronchopathia osteochondroplastica | (Orphanet:3348) |
Williams syndrome | (Orphanet:904) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |