Unossified vertebral bodies

Symptom Information:

Symptom ID: HPO:0004606
Synonyms:
Defect of vertebra ossification [Orphanet:16390]
Unossified vertebral bodies [OMIM:Unossified vertebral bodies]
Lack/delayed ossification of spine/vertebrae [Orphanet:16390]
Unossified vertebral bodies (below level of T12) [OMIM:Unossified vertebral bodies (below level of T12)]
Quality:
Cross references:
HPO:0004599 "Absent or minimally ossified vertebral bodies" [Orphanet:16390]
HPO:0100856 "Poorly ossified vertebrae" [Orphanet:16390]
Orphanet:16390 "Lack/delayed ossification of spine/vertebrae" [Orphanet:16390]
OMIM: "Unossified vertebral bodies" [OMIM:Unossified vertebral bodies]
OMIM: "Unossified vertebral bodies (below level of T12)" [OMIM:Unossified vertebral bodies (below level of T12)]
Is a (Direct Parents):
Orphanet Abnormal form of the vertebral bodies
HPO         Absent or minimally ossified vertebral bodies
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 vertebrae(HPO:0003468)
                      Abnormal vertebral ossification(HPO:0100569)
                         Absent or minimally ossified vertebral bodies(HPO:0004599)
                            Unossified vertebral bodies(HPO:0004606)
             Abnormal bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal vertebral ossification(HPO:0100569)
                      Absent or minimally ossified vertebral bodies(HPO:0004599)
                         Unossified vertebral bodies(HPO:0004606)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Diaphanospondylodysostosis (Orphanet:66637)
Perinatal lethal hypophosphatasia (Orphanet:247623)