Hypoplastic vertebral bodies

Symptom Information:

Symptom ID: HPO:0008479
Synonyms:
Hypoplastic vertebral bodies [OMIM:Hypoplastic vertebral bodies]
Quality:
Cross references:
OMIM: "Hypoplastic vertebral bodies" [OMIM:Hypoplastic vertebral bodies]
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)
             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)
                            Hypoplastic vertebral bodies(HPO:0008479)
                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)
                            Hypoplastic vertebral bodies(HPO:0008479)
                   Abnormality of the vertebrae(HPO:0003468)
                      Aplasia/Hypoplasia of the vertebrae(HPO:0008515)
                         Vertebral hypoplasia(HPO:0008417)
                            Hypoplastic vertebral bodies(HPO:0008479)
             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)
                            Hypoplastic vertebral bodies(HPO:0008479)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Dysosteosclerosis (Orphanet:1782)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
Greenberg dysplasia (Orphanet:1426)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Lethal Kniest-like dysplasia (Orphanet:2347)
Multiple sulfatase deficiency (Orphanet:585)
Opsismodysplasia (Orphanet:2746)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)