Vocal cord paralysis

Symptom Information:

Symptom ID: HPO:0001605
Synonyms:
Vocal cord paralysis [OMIM:Vocal cord paralysis]
Quality:
Cross references:
OMIM: "Vocal cord paralysis" [OMIM:Vocal cord paralysis]
Is a (Direct Parents):
HPO         Bilateral vocal cord paralysis
HPO         Vocal cord paresis
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)
                   Vocal cord paralysis(HPO:0001605)
       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)
                      Hoarse voice(HPO:0001609)
                         Vocal cord paresis(HPO:0001604)
                            Vocal cord paralysis(HPO:0001605)
                   Abnormality of the vocal cords(HPO:0008777)
                      Vocal cord paresis(HPO:0001604)
                         Vocal cord paralysis(HPO:0001605)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Distal hereditary motor neuropathy type 7 (Orphanet:139589)
FEINGOLD SYNDROME 1 (OMIM:164280)
Feingold syndrome (Orphanet:1305)
Hereditary neuropathy with liability to pressure palsies (Orphanet:640)
Laryngeal abductor paralysis (Orphanet:2808)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB (OMIM:607641)
PARAGANGLIOMAS 1 (OMIM:168000)
PARAGANGLIOMAS 2 (OMIM:601650)
PARAGANGLIOMAS 3 (OMIM:605373)
Ptosis - vocal cord paralysis (Orphanet:2997)
Riboflavin transporter deficiency (Orphanet:97229)
Williams syndrome (Orphanet:904)