Abnormality of the voice

Symptom Information:

Symptom ID: HPO:0001608
Synonyms:
Voice abnormality [HPO:0001608]
Abnormal voice [Orphanet:33750]
Abnormal voice (finding) [Orphanet:33750]
Voice Disturbance [Orphanet:33750]
Abnormal cry/voice/phonation disorder/nasal speech [Orphanet:33750]
Voice disturbance, unspecified [Orphanet:33750]
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]
Abnormal voice [OMIM:Abnormal voice]
Hoarseness (53%) [OMIM:Hoarseness (53%)]
Abnormal cry [Orphanet:33750]
Phonation disorder [Orphanet:33750]
Voice impairment [Orphanet:33750]
Voice Disorders [Orphanet:33750]
Quality:
Cross references:
Orphanet:33750 "Abnormal cry/voice/phonation disorder/nasal speech" [Orphanet:33750]
OMIM: "Abnormal voice" [OMIM:Abnormal voice]
OMIM: "Hoarseness (53%)" [OMIM:Hoarseness (53%)]
UMLS:C1527340 "Voice Disturbance" [Orphanet:33750]
UMLS:C0042940 "Voice Disorders" [Orphanet:33750]
Is a (Direct Parents):
Orphanet Abnormality of the respiratory system
HPO         Abnormality of the larynx
MedDRA Upper respiratory tract signs and symptoms
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)
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)