Shield chest

Symptom Information:

Symptom ID: HPO:0000914
Synonyms:
Barrel chest [Orphanet:15320]
Barrel chest (disorder) [Orphanet:15320]
Shield chest [OMIM:Shield chest]
Flared chest/bell-shaped thorax/shield chest [Orphanet:15320]
Barrel chest [MedDRA:10004133]
Quality:
Cross references:
HPO:0001552 "Barrel-shaped chest" [Orphanet:15320]
Orphanet:15320 "Flared chest/bell-shaped thorax/shield chest" [Orphanet:15320]
OMIM: "Shield chest" [OMIM:Shield chest]
UMLS:C0264172 "Barrel chest" [Orphanet:15320]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
HPO         Enlarged thorax
MedDRA Trunk deformities
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the thorax(HPO:0000765)
                   Abnormality of the rib cage(HPO:0001547)
                      Enlarged thorax(HPO:0100625)
                         Shield chest(HPO:0000914)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Trunk deformities(MedDRA:10064466)
          Shield chest(HPO:0000914)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion (Orphanet:231130)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
Fucosidosis (Orphanet:349)
Hurler-Scheie syndrome (Orphanet:93476)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
LEOPARD SYNDROME 3 (OMIM:613707)
NOONAN SYNDROME 1 (OMIM:163950)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
Spondylo-ocular syndrome (Orphanet:85194)
Subaortic stenosis - short stature (Orphanet:3191)
Wolcott-Rallison syndrome (Orphanet:1667)