Bell-shaped thorax
Symptom Information:
Symptom ID: | HPO:0001591 | |||||||||
Synonyms: |
|
|||||||||
Quality: | ||||||||||
Cross references: |
|
|||||||||
Is a (Direct Parents): |
|
|||||||||
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) |