Tracheomalacia

Symptom Information:

Symptom ID: HPO:0002779
Synonyms:
Tracheomalacia (disorder) [Orphanet:32280]
Tracheomalacia [Orphanet:32280]
Tracheomalacia [OMIM:Tracheomalacia]
Tracheomalacia/tracheobronchomalacia [Orphanet:32280]
Tracheomalacia [MedDRA:10056397]
Tracheomalacia (excl congenital) [MedDRA:10056397]
Acquired tracheobronchomalacia [MedDRA:10056397]
Tracheomalacia (tracheostomy may be required) [OMIM:Tracheomalacia (tracheostomy may be required)]
Quality:
Cross references:
Orphanet:32280 "Tracheomalacia/tracheobronchomalacia" [Orphanet:32280]
OMIM: "Tracheomalacia" [OMIM:Tracheomalacia]
OMIM: "Tracheomalacia (tracheostomy may be required)" [OMIM:Tracheomalacia (tracheostomy may be required)]
UMLS:C0948187 "Tracheomalacia" [HPO:0002779]
UMLS:C0948187 "Tracheomalacia" [Orphanet:32280]
Is a (Direct Parents):
Orphanet Abnormality of the diaphragm
MedDRA Respiratory complications associated with device
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)
                      Tracheomalacia(HPO:0002779)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    Complications associated with device(MedDRA:10069781)
       Respiratory complications associated with device(MedDRA:10069788)
          Tracheomalacia(HPO:0002779)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

2q37 microdeletion syndrome (Orphanet:1001)
Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Autosomal dominant Larsen syndrome (Orphanet:503)
Campomelic dysplasia (Orphanet:140)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Costello syndrome (Orphanet:3071)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (Orphanet:221145)
Diaphanospondylodysostosis (Orphanet:66637)
Goldenhar syndrome (Orphanet:374)
Hallermann-Streiff syndrome (Orphanet:2108)
Kleefstra syndrome (Orphanet:261494)
Kniest dysplasia (Orphanet:485)
Lethal Larsen-like syndrome (Orphanet:2371)
MEIER-GORLIN SYNDROME 2 (OMIM:613800)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Relapsing polychondritis (Orphanet:728)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Waardenburg syndrome type 3 (Orphanet:896)