Barrel-shaped chest
Symptom Information:
Symptom ID: | HPO:0001552 | ||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |