Nasal speech
Symptom Information:
Symptom ID: | HPO:0001611 | ||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||
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) Nasal speech(HPO:0001611) MedDRA: |
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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) |