Laryngeal stenosis
Symptom Information:
Symptom ID: | HPO:0001602 | |||||||||||||
Synonyms: |
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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) 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) |
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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) |