Barrel-shaped chest

Symptom Information:

Symptom ID: HPO:0001552
Synonyms:
Barrel chest [HPO:0001552]
Broad chest [HPO:0001552]
Wide rib cage [Orphanet:15120]
Barrel chest [Orphanet:15320]
Barrel chest (disorder) [Orphanet:15320]
Barrel chest [OMIM:Barrel chest]
Barrel-shaped chest [OMIM:Barrel-shaped chest]
Broad chest [OMIM:Broad chest]
Wide rib cage/thorax [Orphanet:15120]
Flared chest/bell-shaped thorax/shield chest [Orphanet:15320]
Barrel chest [MedDRA:10004133]
Barrel-shaped chest (more prominent in adults) [OMIM:Barrel-shaped chest (more prominent in adults)]
Broad chest (male) [OMIM:Broad chest (male)]
Broad chest (neonate) [OMIM:Broad chest (neonate)]
Quality:
Cross references:
HPO:0100625 "Enlarged thorax" [Orphanet:15120]
HPO:0000914 "Shield chest" [Orphanet:15320]
Orphanet:15120 "Wide rib cage/thorax" [Orphanet:15120]
Orphanet:15320 "Flared chest/bell-shaped thorax/shield chest" [Orphanet:15320]
OMIM: "Barrel chest" [OMIM:Barrel chest]
OMIM: "Barrel-shaped chest" [OMIM:Barrel-shaped chest]
OMIM: "Broad chest" [OMIM:Broad chest]
OMIM: "Barrel-shaped chest (more prominent in adults)" [OMIM:Barrel-shaped chest (more prominent in adults)]
OMIM: "Broad chest (male)" [OMIM:Broad chest (male)]
OMIM: "Broad chest (neonate)" [OMIM:Broad chest (neonate)]
UMLS:C0264172 "Barrel chest" [Orphanet:15320]
Is a (Direct Parents):
Orphanet Shield chest
MedDRA Trunk deformities
HPO         Enlarged thorax
Orphanet Abnormality of the thorax
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)
                         Barrel-shaped chest(HPO:0001552)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Trunk deformities(MedDRA:10064466)
          Barrel-shaped chest(HPO:0001552)
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 2 (Orphanet:93296)
Autosomal dominant brachyolmia (Orphanet:93304)
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY (OMIM:210550)
Brachyolmia (Orphanet:1293)
CHST3-related skeletal dysplasia (Orphanet:263463)
Costello syndrome (Orphanet:3071)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
Fucosidosis (Orphanet:349)
Greenberg dysplasia (Orphanet:1426)
Hypochondrogenesis (Orphanet:93297)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
KETOADIPICACIDURIA (OMIM:245130)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
Osteoporosis - pseudoglioma (Orphanet:2788)
Phocomelia, Schinzel type (Orphanet:2879)
SCARF syndrome (Orphanet:3134)
SMITH-MCCORT DYSPLASIA 2 (OMIM:615222)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT (OMIM:184100)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
Smith-McCort dysplasia (Orphanet:178355)
Spondyloepimetaphyseal dysplasia, aggrecan type (Orphanet:171866)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)
Subaortic stenosis - short stature (Orphanet:3191)
Wolcott-Rallison syndrome (Orphanet:1667)