Posterior vertebral hypoplasia

Symptom Information:

Symptom ID: HPO:0008451
Synonyms:
Posterior vertebral hypoplasia [OMIM:Posterior vertebral hypoplasia]
Quality:
Cross references:
OMIM: "Posterior vertebral hypoplasia" [OMIM:Posterior vertebral hypoplasia]
Is a (Direct Parents):
HPO         Vertebral hypoplasia
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)
             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 vertebrae(HPO:0008515)
                         Vertebral hypoplasia(HPO:0008417)
                            Posterior vertebral hypoplasia(HPO:0008451)
             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 vertebrae(HPO:0008515)
                         Vertebral hypoplasia(HPO:0008417)
                            Posterior vertebral hypoplasia(HPO:0008451)
                Abnormality of the vertebral column(HPO:0000925)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Aplasia/Hypoplasia of the vertebrae(HPO:0008515)
                         Vertebral hypoplasia(HPO:0008417)
                            Posterior vertebral hypoplasia(HPO:0008451)
                   Abnormality of the vertebrae(HPO:0003468)
                      Aplasia/Hypoplasia of the vertebrae(HPO:0008515)
                         Vertebral hypoplasia(HPO:0008417)
                            Posterior vertebral hypoplasia(HPO:0008451)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

FIBROCHONDROGENESIS 1 (OMIM:228520)
Fibrochondrogenesis (Orphanet:2021)