Shield chest
Symptom Information:
Symptom ID: | HPO:0000914 | ||||||
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) 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) |
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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) |