Abnormality of the voice
Symptom Information:
Symptom ID: | HPO:0001608 | |||||||||||||||||||||||||||||
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 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) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Respiratory disorders NEC(MedDRA:10038716) Upper respiratory tract signs and symptoms(MedDRA:10046313) Abnormality of the voice(HPO:0001608) |
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Database Frequency: | 126 / 7739 | |||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
22q11.2 deletion syndrome | (Orphanet:567) |
22q11.2 microduplication syndrome | (Orphanet:1727) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
3q29 microdeletion syndrome | (Orphanet:65286) |
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency | (Orphanet:753) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
Acromegaly | (Orphanet:963) |
Acromicric dysplasia | (Orphanet:969) |
Acroosteolysis, dominant type | (Orphanet:955) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Antisynthetase syndrome | (Orphanet:81) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Bloom syndrome | (Orphanet:125) |
Braddock syndrome | (Orphanet:52047) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION | (OMIM:215480) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Central congenital hypothyroidism | (Orphanet:226298) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Cherubism | (Orphanet:184) |
Classic galactosemia | (Orphanet:79239) |
Cleft palate-lateral synechia syndrome | (Orphanet:2016) |
Cohen syndrome | (Orphanet:193) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital hypothyroidism due to developmental anomaly | (Orphanet:95711) |
Congenital laryngeal web | (Orphanet:2374) |
Congenital laryngomalacia | (Orphanet:2373) |
Congenital velopharyngeal incompetence | (Orphanet:2291) |
Cornelia de Lange syndrome | (Orphanet:199) |
Corpus callosum agenesis - double urinary collecting system | (Orphanet:1492) |
Cryptorchidism - arachnodactyly - intellectual deficit | (Orphanet:1548) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
Cystinosis | (Orphanet:213) |
Dermatomyositis | (Orphanet:221) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Dysmorphism - short stature - deafness - disorder of sex development | (Orphanet:2282) |
Early-onset generalized limb-onset dystonia | (Orphanet:256) |
Edinburgh malformation syndrome | (Orphanet:1895) |
Esophageal carcinoma | (Orphanet:70482) |
Esophageal squamous cell carcinoma | (Orphanet:99977) |
FACES syndrome | (Orphanet:1969) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Farber lipogranulomatosis | (Orphanet:333) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Floating-Harbor syndrome | (Orphanet:2044) |
Foix-Chavany-Marie syndrome | (Orphanet:2048) |
Galactosemia | (Orphanet:352) |
Geleophysic dysplasia | (Orphanet:2623) |
Growth hormone insensitivity syndrome | (Orphanet:181393) |
HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES | (OMIM:239350) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Huntington disease | (Orphanet:399) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
Hypogonadotropic hypogonadism - frontoparietal alopecia | (Orphanet:2230) |
Hypothyroidism due to TSH receptor mutations | (Orphanet:90673) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Infant botulism | (Orphanet:178478) |
Infantile symmetrical thalamic degeneration | (Orphanet:3311) |
Infantile thalamic degeneration | (Orphanet:1577) |
Intellectual deficit - hypoplastic corpus callosum - preauricular tag | (Orphanet:1495) |
Intellectual deficit, X-linked - short stature - obesity | (Orphanet:3055) |
Juvenile dermatomyositis | (Orphanet:93672) |
Kallmann syndrome | (Orphanet:478) |
Keipert syndrome | (Orphanet:2662) |
Keutel syndrome | (Orphanet:85202) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LOC syndrome | (Orphanet:2407) |
Laron syndrome | (Orphanet:633) |
Laryngeal abductor paralysis - intellectual deficit | (Orphanet:2375) |
Laryngo-tracheo-esophageal cleft | (Orphanet:2004) |
Larynx atresia | (Orphanet:1202) |
Lipoid proteinosis | (Orphanet:530) |
Locked-in syndrome | (Orphanet:2406) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Maple syrup urine disease | (Orphanet:511) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Moebius syndrome | (Orphanet:570) |
Monosomy 5p | (Orphanet:281) |
Muckle-Wells syndrome | (Orphanet:575) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mulibrey nanism | (Orphanet:2576) |
Muscle-eye-brain disease | (Orphanet:588) |
Myhre syndrome | (Orphanet:2588) |
Myotonia permanens | (Orphanet:99735) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Permanent congenital hypothyroidism | (Orphanet:226292) |
Pfeiffer-Palm-Teller syndrome | (Orphanet:2871) |
Polymyositis | (Orphanet:732) |
Primary basilar impression | (Orphanet:2285) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Ptosis - vocal cord paralysis | (Orphanet:2997) |
Relapsing polychondritis | (Orphanet:728) |
Rett syndrome | (Orphanet:778) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
STUTTERING, FAMILIAL PERSISTENT, 1 | (OMIM:184450) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Magenis syndrome | (Orphanet:819) |
Subaortic stenosis - short stature | (Orphanet:3191) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Symmetrical thalamic calcifications | (Orphanet:1314) |
Tumoral calcinosis | (Orphanet:53715) |
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME | (OMIM:300280) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |
Weaver syndrome | (Orphanet:3447) |
Werner syndrome | (Orphanet:902) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
Xq27.3q28 duplication syndrome | (Orphanet:261483) |