Hypoplastic sacrum

Symptom Information:

Symptom ID: HPO:0004590
Synonyms:
Hypoplastic sacrum [OMIM:Hypoplastic sacrum]
Quality:
Cross references:
OMIM: "Hypoplastic sacrum" [OMIM:Hypoplastic sacrum]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the sacrum
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)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Hypoplastic sacrum(HPO:0004590)
                Abnormality of the vertebral column(HPO:0000925)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Hypoplastic sacrum(HPO:0004590)
                   Abnormality of the sacrum(HPO:0005107)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Hypoplastic sacrum(HPO:0004590)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Hypoplastic sacrum(HPO:0004590)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive Robinow syndrome (Orphanet:1507)
Brachydactyly type B (Orphanet:93383)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)