Vertebral hypoplasia

Symptom Information:

Symptom ID: HPO:0008417
Synonyms:
Underdeveloped vertebrae [HPO:0008417]
Underdeveloped vertebrae [OMIM:Underdeveloped vertebrae]
Vertebral hypoplasia [OMIM:Vertebral hypoplasia]
Quality:
Cross references:
OMIM: "Underdeveloped vertebrae" [OMIM:Underdeveloped vertebrae]
OMIM: "Vertebral hypoplasia" [OMIM:Vertebral hypoplasia]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the vertebrae
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)
             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)
                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)
                   Abnormality of the vertebrae(HPO:0003468)
                      Aplasia/Hypoplasia of the vertebrae(HPO:0008515)
                         Vertebral hypoplasia(HPO:0008417)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
CHILD syndrome (Orphanet:139)
Goldenhar syndrome (Orphanet:374)
Mucopolysaccharidosis type 2 (Orphanet:580)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
VERTEBRAL HYPOPLASIA WITH LUMBAR KYPHOSIS (OMIM:192900)