Laryngeal stenosis

Symptom Information:

Symptom ID: HPO:0001602
Synonyms:
Larynx stenosis [Orphanet:32160]
Stenosis of larynx (disorder) [Orphanet:32160]
Laryngostenosis [Orphanet:32160]
Laryngeal stenosis [OMIM:Laryngeal stenosis]
Larynx/laryngeal stenosis/atresia [Orphanet:32160]
Laryngeal stenosis [Orphanet:32160]
Laryngeal stenosis [MedDRA:10023862]
Laryngeal stricture [MedDRA:10023862]
Stenosis of larynx [MedDRA:10023862]
Subglottic stenosis [MedDRA:10023862]
Supraglottic stenosis [MedDRA:10023862]
Laryngeal stenosis (in some patients) [OMIM:Laryngeal stenosis (in some patients)]
Subglottic stenosis (variable) [OMIM:Subglottic stenosis (variable)]
Quality:
Cross references:
Orphanet:32160 "Larynx/laryngeal stenosis/atresia" [Orphanet:32160]
OMIM: "Laryngeal stenosis" [OMIM:Laryngeal stenosis]
OMIM: "Laryngeal stenosis (in some patients)" [OMIM:Laryngeal stenosis (in some patients)]
OMIM: "Subglottic stenosis (variable)" [OMIM:Subglottic stenosis (variable)]
UMLS:C0023075 "Laryngostenosis" [Orphanet:32160]
Is a (Direct Parents):
MedDRA Laryngeal spasm, oedema and obstruction
HPO         Abnormality of the larynx
Orphanet Abnormality of the diaphragm
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)
                   Laryngeal stenosis(HPO:0001602)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Upper respiratory tract disorders (excl infections)(MedDRA:10046304)
       Laryngeal spasm, oedema and obstruction(MedDRA:10023855)
          Laryngeal stenosis(HPO:0001602)
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Atelosteogenesis type I (Orphanet:1190)
Braddock syndrome (Orphanet:52047)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Dystrophic epidermolysis bullosa (Orphanet:303)
Fraser syndrome (Orphanet:2052)
Frontometaphyseal dysplasia (Orphanet:1826)
Geleophysic dysplasia (Orphanet:2623)
Junctional epidermolysis bullosa (Orphanet:305)
Kindler syndrome (Orphanet:2908)
Leri pleonosteosis (Orphanet:2900)
Matthew-Wood syndrome (Orphanet:2470)
Mucopolysaccharidosis type 2 (Orphanet:580)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM (OMIM:614501)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
THORACOLARYNGOPELVIC DYSPLASIA (OMIM:187760)
Tetraamelia - multiple malformations (Orphanet:3301)
Thoracolaryngopelvic dysplasia (Orphanet:3317)
Toriello-Carey syndrome (Orphanet:3338)
VACTERL/VATER association (Orphanet:887)