Vocal cord paresis
Symptom Information:
Symptom ID: | HPO:0001604 | ||||||||||||
Synonyms: |
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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 nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Vocal cord paresis(HPO:0001604) 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 vocal cords(HPO:0008777) Vocal cord paresis(HPO:0001604) Abnormality of the voice(HPO:0001608) Hoarse voice(HPO:0001609) Vocal cord paresis(HPO:0001604) MedDRA: Nervous system disorders(MedDRA:10029205) Cranial nerve disorders (excl neoplasms)(MedDRA:10011305) Vagus nerve disorders(MedDRA:10046967) Vocal cord paresis(HPO:0001604) |
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Database Frequency: | 8 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE | (OMIM:607706) |
CODAS syndrome | (Orphanet:1458) |
Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
Distal hereditary motor neuropathy type 7 | (Orphanet:139589) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA | (OMIM:158580) |