Abnormality of the sacrum

Symptom Information:

Symptom ID: HPO:0005107
Sacrococcygeal anomaly [Orphanet:16630]
Sacro-coccyx/sacrum anomaly [Orphanet:16630]
Cross references:
Orphanet:16630 "Sacro-coccyx/sacrum anomaly" [Orphanet:16630]
Is a (Direct Parents):
Orphanet Abnormality of the vertebral column
HPO         Abnormality of the vertebral column
HPO         Unossified sacrum
Is a (Whole tree): HPO:
    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)
Database Frequency: 18 / 7739

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-K├╝ster-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)