Rib fusion

Symptom Information:

Symptom ID: HPO:0000902
Synonyms:
Fused ribs [HPO:0000902]
Fused ribs [OMIM:Fused ribs]
Rib fusion [OMIM:Rib fusion]
Rib fusion (100%) [OMIM:Rib fusion (100%)]
Rib fusion (variable) [OMIM:Rib fusion (variable)]
Quality:
Cross references:
OMIM: "Fused ribs" [OMIM:Fused ribs]
OMIM: "Rib fusion" [OMIM:Rib fusion]
OMIM: "Rib fusion (100%)" [OMIM:Rib fusion (100%)]
OMIM: "Rib fusion (variable)" [OMIM:Rib fusion (variable)]
Is a (Direct Parents):
HPO         Abnormality of the ribs
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:
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)