Absent or minimally ossified vertebral bodies
Symptom Information:
Symptom ID: | HPO:0004599 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 bone structure(HPO:0003330) Abnormal bone ossification(HPO:0011849) Abnormal vertebral ossification(HPO:0100569) Absent or minimally ossified vertebral bodies(HPO:0004599) 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) MedDRA: |
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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) |