Nasal, dysarthic speech

Symptom Information:

Symptom ID: HPO:0008376
Synonyms:
Nasal voice [Orphanet:33750]
Nasal voice (finding) [Orphanet:33750]
Nasal, dysarthic speech [OMIM:Nasal, dysarthic speech]
Abnormal cry/voice/phonation disorder/nasal speech [Orphanet:33750]
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:0001611 "Nasal speech" [Orphanet:33750]
HPO:0100271 "Hyponasal speech" [Orphanet:33750]
HPO:0001614 "Hypernasal speech" [Orphanet:33750]
Orphanet:33750 "Abnormal cry/voice/phonation disorder/nasal speech" [Orphanet:33750]
OMIM: "Nasal, dysarthic speech" [OMIM:Nasal, dysarthic speech]
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 respiratory system
Orphanet Abnormality of the voice
HPO         Dysarthria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Neurological speech impairment(HPO:0002167)
                   Dysarthria(HPO:0001260)
                      Nasal, dysarthic speech(HPO:0008376)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
Autosomal dominant limb-girdle muscular dystrophy type 1A (Orphanet:266)
Bloom syndrome (Orphanet:125)
Buschke-Ollendorff syndrome (Orphanet:1306)
Huntington disease (Orphanet:399)
Maple syrup urine disease (Orphanet:511)
Werner syndrome (Orphanet:902)
Wilson-Turner syndrome (Orphanet:3459)