Bell-shaped thorax

Symptom Information:

Symptom ID: HPO:0001591
Synonyms:
Bell-shaped chest [HPO:0001591]
Constricted, bell-shaped thorax [HPO:0001591]
Narrow, bell-shaped thorax [HPO:0001591]
Bell shaped thorax [Orphanet:15320]
Bell-shaped chest [OMIM:Bell-shaped chest]
Bell-shaped thorax [OMIM:Bell-shaped thorax]
Constricted, bell-shaped thorax [OMIM:Constricted, bell-shaped thorax]
Narrow, bell-shaped thorax [OMIM:Narrow, bell-shaped thorax]
Flared chest/bell-shaped thorax/shield chest [Orphanet:15320]
Quality:
Cross references:
Orphanet:15320 "Flared chest/bell-shaped thorax/shield chest" [Orphanet:15320]
OMIM: "Bell-shaped chest" [OMIM:Bell-shaped chest]
OMIM: "Bell-shaped thorax" [OMIM:Bell-shaped thorax]
OMIM: "Constricted, bell-shaped thorax" [OMIM:Constricted, bell-shaped thorax]
OMIM: "Narrow, bell-shaped thorax" [OMIM:Narrow, bell-shaped thorax]
Is a (Direct Parents):
HPO         Abnormality of the rib cage
Orphanet Shield chest
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)
                      Bell-shaped thorax(HPO:0001591)
MedDRA:
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

Antenatal multiminicore disease with arthrogryposis multiplex congenita (Orphanet:178148)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Chondrodysplasia - disorder of sex development (Orphanet:1422)
Craniomicromelic syndrome (Orphanet:1524)
Desbuquois syndrome (Orphanet:1425)
Diaphanospondylodysostosis (Orphanet:66637)
FGFR2-related bent bone dysplasia (Orphanet:313855)
FIBROCHONDROGENESIS 2 (OMIM:614524)
Fibrochondrogenesis (Orphanet:2021)
Joubert syndrome 21 (OMIM:615636)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
Mulibrey nanism (Orphanet:2576)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Opsismodysplasia (Orphanet:2746)
Osteocraniostenosis (Orphanet:2763)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Pelviscapular dysplasia (Orphanet:93333)
Richieri Costa-da Silva syndrome (Orphanet:3101)
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE (OMIM:611702)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Short-rib thoracic dysplasia 11 with or without polydactyly (OMIM:615633)
Short-rib thoracic dysplasia 13 with or without polydactyly (OMIM:616300)
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Orphanet:93358)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
THORACIC DYSOSTOSIS, ISOLATED (OMIM:187750)
THORACOLARYNGOPELVIC DYSPLASIA (OMIM:187760)
Thoracolaryngopelvic dysplasia (Orphanet:3317)
Thoracomelic dysplasia (Orphanet:1803)
Zellweger syndrome (Orphanet:912)