Tracheal stenosis
Symptom Information:
Symptom ID: | HPO:0002777 | |||||||
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 respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of the upper respiratory tract(HPO:0002087) Abnormality of the tracheobronchial system(HPO:0005607) Abnormality of the trachea(HPO:0002778) Tracheal stenosis(HPO:0002777) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Upper respiratory tract disorders (excl infections)(MedDRA:10046304) Tracheal disorders (excl infections and neoplasms)(MedDRA:10044288) Tracheal stenosis(HPO:0002777) |
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Database Frequency: | 35 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS | (OMIM:601427) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Congenital bronchobiliary fistula | (Orphanet:2040) |
Diabetic embryopathy | (Orphanet:1926) |
Fraser syndrome | (Orphanet:2052) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
GELEOPHYSIC DYSPLASIA 1 | (OMIM:231050) |
Geleophysic dysplasia | (Orphanet:2623) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hydrolethalus | (Orphanet:2189) |
Hypomandibular faciocranial dysostosis | (Orphanet:1790) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Jung-Wolff-Back-Stahl syndrome | (Orphanet:2321) |
Keutel syndrome | (Orphanet:85202) |
Kniest dysplasia | (Orphanet:485) |
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia | (Orphanet:2005) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Pendred syndrome | (Orphanet:705) |
Relapsing polychondritis | (Orphanet:728) |
Scheie syndrome | (Orphanet:93474) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
Toriello-Carey syndrome | (Orphanet:3338) |
Tracheal agenesis | (Orphanet:3346) |
Tracheobronchomegaly | (Orphanet:3347) |
VACTERL/VATER association | (Orphanet:887) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |