Nasal speech

Symptom Information:

Symptom ID: HPO:0001611
Synonyms:
Hypernasal speech [HPO:0001611]
Hypernasal voice [HPO:0001611]
Nasal voice [HPO:0001611]
Nasal voice [Orphanet:33750]
Nasal voice (finding) [Orphanet:33750]
Hypernasal speech [OMIM:Hypernasal speech]
Hypernasal voice [OMIM:Hypernasal voice]
Nasal speech [OMIM:Nasal speech]
Nasal voice [OMIM:Nasal voice]
Abnormal cry/voice/phonation disorder/nasal speech [Orphanet:33750]
Hypernasal voice (in some patients) [OMIM:Hypernasal voice (in some patients)]
Nasal speech (50%) [OMIM:Nasal speech (50%)]
Nasal speech (HCS) [OMIM:Nasal speech (HCS)]
Nasal voice (in some patients) [OMIM:Nasal voice (in some patients)]
Abnormal cry [Orphanet:33750]
Phonation disorder [Orphanet:33750]
Voice impairment [Orphanet:33750]
Voice Disorders [Orphanet:33750]
Quality:
Cross references:
HPO:0100271 "Hyponasal speech" [Orphanet:33750]
HPO:0001614 "Hypernasal speech" [Orphanet:33750]
HPO:0008376 "Nasal, dysarthic speech" [Orphanet:33750]
Orphanet:33750 "Abnormal cry/voice/phonation disorder/nasal speech" [Orphanet:33750]
OMIM: "Hypernasal speech" [OMIM:Hypernasal speech]
OMIM: "Hypernasal voice" [OMIM:Hypernasal voice]
OMIM: "Nasal speech" [OMIM:Nasal speech]
OMIM: "Nasal voice" [OMIM:Nasal voice]
OMIM: "Hypernasal voice (in some patients)" [OMIM:Hypernasal voice (in some patients)]
OMIM: "Nasal speech (50%)" [OMIM:Nasal speech (50%)]
OMIM: "Nasal speech (HCS)" [OMIM:Nasal speech (HCS)]
OMIM: "Nasal voice (in some patients)" [OMIM:Nasal voice (in some patients)]
UMLS:C0566620 "Nasal voice" [Orphanet:33750]
UMLS:C0042940 "Voice Disorders" [Orphanet:33750]
Is a (Direct Parents):
Orphanet Abnormality of the voice
Orphanet Abnormality of the respiratory system
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)
                      Nasal speech(HPO:0001611)
MedDRA:
Database Frequency: 48 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
22q11.2 microduplication syndrome (Orphanet:1727)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2p21 microdeletion syndrome (Orphanet:163693)
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Bloom syndrome (Orphanet:125)
Branchio-oculo-facial syndrome (Orphanet:1297)
Buschke-Ollendorff syndrome (Orphanet:1306)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Classic multiminicore myopathy (Orphanet:324604)
Cold-induced sweating syndrome (Orphanet:157820)
DIGEORGE SYNDROME (OMIM:188400)
Freeman-Sheldon syndrome (Orphanet:2053)
Huntington disease (Orphanet:399)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
Kearns-Sayre syndrome (Orphanet:480)
Keutel syndrome (Orphanet:85202)
Koolen-De Vries syndrome (Orphanet:96169)
LUJAN-FRYNS SYNDROME (OMIM:309520)
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 (OMIM:300676)
MYASTHENIA GRAVIS (OMIM:254200)
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET (OMIM:614399)
Maple syrup urine disease (Orphanet:511)
Mesomelia-synostoses syndrome (Orphanet:2496)
Microduplication Xp11.22-p11.23 syndrome (Orphanet:217377)
Muscular dystrophy, Selcen type (Orphanet:199340)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Oculopharyngodistal myopathy (Orphanet:98897)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Prader-Willi syndrome (Orphanet:739)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)
Renpenning syndrome (Orphanet:3242)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
Spheroid body myopathy (Orphanet:268129)
Stüve-Wiedemann syndrome (Orphanet:3206)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
Velo-facial-skeletal syndrome (Orphanet:3424)
Werner syndrome (Orphanet:902)
Wilson-Turner syndrome (Orphanet:3459)
Wrinkly skin syndrome (Orphanet:2834)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)