Absent or minimally ossified vertebral bodies

Symptom Information:

Symptom ID: HPO:0004599
Synonyms:
Defect of vertebra ossification [Orphanet:16390]
Absent or minimally ossified vertebral bodies [OMIM:Absent or minimally ossified vertebral bodies]
Lack/delayed ossification of spine/vertebrae [Orphanet:16390]
Quality:
Cross references:
HPO:0004606 "Unossified vertebral bodies" [Orphanet:16390]
HPO:0100856 "Poorly ossified vertebrae" [Orphanet:16390]
Orphanet:16390 "Lack/delayed ossification of spine/vertebrae" [Orphanet:16390]
OMIM: "Absent or minimally ossified vertebral bodies" [OMIM:Absent or minimally ossified vertebral bodies]
Is a (Direct Parents):
HPO         Abnormal vertebral ossification
HPO         Absent ossification of thoracic vertebral bodies
Orphanet Abnormal form of the 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)
             Abnormal bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal vertebral ossification(HPO:0100569)
                      Absent or minimally ossified vertebral bodies(HPO:0004599)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis type 1B (Orphanet:93298)
Boomerang dysplasia (Orphanet:1263)
Campomelia, Cumming type (Orphanet:1318)
Campomelic dysplasia (Orphanet:140)
Cartilage-hair hypoplasia (Orphanet:175)
Crane-Heise syndrome (Orphanet:1512)
Greenberg dysplasia (Orphanet:1426)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Lichstenstein syndrome (Orphanet:2390)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Opsismodysplasia (Orphanet:2746)
Parastremmatic dwarfism (Orphanet:2646)
Primary hyperoxaluria (Orphanet:416)
Pyknoachondrogenesis (Orphanet:3003)
Schwartz-Jampel syndrome (Orphanet:800)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Tetraamelia - multiple malformations (Orphanet:3301)