Abnormality of the sacrum
Symptom Information:
Symptom ID: | HPO:0005107 | ||||||
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 vertebral column(HPO:0000925) Abnormality of the sacrum(HPO:0005107) MedDRA: |
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Database Frequency: | 18 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant spondylocostal dysostosis | (Orphanet:1797) |
Bilateral renal agenesis | (Orphanet:1848) |
Caudal duplication | (Orphanet:1756) |
Cleidocranial dysplasia | (Orphanet:1452) |
Crouzon disease | (Orphanet:207) |
Crouzon syndrome - acanthosis nigricans | (Orphanet:93262) |
Diabetic embryopathy | (Orphanet:1926) |
Femoral-facial syndrome | (Orphanet:1988) |
Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
Infantile myofibromatosis | (Orphanet:2591) |
Isolated Klippel-Feil syndrome | (Orphanet:2345) |
Mayer-Rokitansky-Küster-Hauser syndrome | (Orphanet:3109) |
Pyknoachondrogenesis | (Orphanet:3003) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Sacrococcygeal dysgenesis association | (Orphanet:1773) |
Skeletal dysplasia - intellectual deficit | (Orphanet:1436) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
VACTERL/VATER association | (Orphanet:887) |