Rib fusion
Symptom Information:
Symptom ID: | HPO:0000902 | |||||
Synonyms: |
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Quality: | ||||||
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) Abnormality of the ribs(HPO:0000772) Rib fusion(HPO:0000902) MedDRA: |
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Database Frequency: | 19 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Aicardi syndrome | (Orphanet:50) |
Anophthalmia/microphthalmia - esophageal atresia | (Orphanet:77298) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
Baller-Gerold syndrome | (Orphanet:1225) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Femoral-facial syndrome | (Orphanet:1988) |
KBG syndrome | (Orphanet:2332) |
Pallister-Hall syndrome | (Orphanet:672) |
Poland syndrome | (Orphanet:2911) |
Pontine tegmental cap dysplasia | (Orphanet:269229) |
SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE | (OMIM:277300) |
SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE | (OMIM:608681) |
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE | (OMIM:613686) |
Spondylocostal dysostosis - anal and genitourinary malformations | (Orphanet:94095) |
TMCO1 defect syndrome | (Orphanet:228407) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |