Tracheal stenosis

Symptom Information:

Symptom ID: HPO:0002777
Synonyms:
Stenosis of trachea (disorder) [Orphanet:32240]
Tracheal Stenosis [Orphanet:32240]
Tracheal stenosis [OMIM:Tracheal stenosis]
Tracheal atresia/stenosis [Orphanet:32240]
Tracheal stenosis [Orphanet:32240]
Tracheal stenosis [MedDRA:10050816]
Tracheal stenosis (male) [OMIM:Tracheal stenosis (male)]
Quality:
Cross references:
Orphanet:32240 "Tracheal atresia/stenosis" [Orphanet:32240]
OMIM: "Tracheal stenosis" [OMIM:Tracheal stenosis]
OMIM: "Tracheal stenosis (male)" [OMIM:Tracheal stenosis (male)]
UMLS:C0040583 "Tracheal Stenosis" [Orphanet:32240]
Is a (Direct Parents):
Orphanet Abnormality of the diaphragm
MedDRA Tracheal disorders (excl infections and neoplasms)
HPO         Abnormality of the trachea
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)
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)