Hoarse voice

Symptom Information:

Symptom ID: HPO:0001609
Synonyms:
Hoarseness [HPO:0001609]
Husky voice [HPO:0001609]
Hoarse voice [OMIM:Hoarse voice]
Hoarseness [OMIM:Hoarseness]
Husky voice [OMIM:Husky voice]
Hoarseness (53%) [OMIM:Hoarseness (53%)]
Quality:
Cross references:
OMIM: "Hoarse voice" [OMIM:Hoarse voice]
OMIM: "Hoarseness" [OMIM:Hoarseness]
OMIM: "Husky voice" [OMIM:Husky voice]
OMIM: "Hoarseness (53%)" [OMIM:Hoarseness (53%)]
Is a (Direct Parents):
HPO         Abnormality of the voice
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:
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)