Beaking of vertebral bodies

Symptom Information:

Symptom ID: HPO:0004568
Synonyms:
anterior beaking [HPO:0004568]
Anterior beaking of vertebrae [HPO:0004568]
Anterior beaking of vertebral bodies [HPO:0004568]
anterior wedging [HPO:0004568]
Beaked vertebral bodies [HPO:0004568]
Wedged vertebrae [HPO:0004568]
Wedging of vertebra [HPO:0004568]
Anterior beaking of vertebrae [OMIM:Anterior beaking of vertebrae]
Anterior beaking of vertebral bodies [OMIM:Anterior beaking of vertebral bodies]
Anterior wedging [OMIM:Anterior wedging]
Beaked vertebral bodies [OMIM:Beaked vertebral bodies]
Wedged vertebrae [OMIM:Wedged vertebrae]
Anterior beaking (childhood) [OMIM:Anterior beaking (childhood)]
Quality:
Cross references:
OMIM: "Anterior beaking of vertebrae" [OMIM:Anterior beaking of vertebrae]
OMIM: "Anterior beaking of vertebral bodies" [OMIM:Anterior beaking of vertebral bodies]
OMIM: "Anterior wedging" [OMIM:Anterior wedging]
OMIM: "Beaked vertebral bodies" [OMIM:Beaked vertebral bodies]
OMIM: "Wedged vertebrae" [OMIM:Wedged vertebrae]
OMIM: "Anterior beaking (childhood)" [OMIM:Anterior beaking (childhood)]
Is a (Direct Parents):
HPO         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 form of the vertebral bodies(HPO:0003312)
                         Beaking of vertebral bodies(HPO:0004568)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Aspartylglucosaminuria (Orphanet:93)
Autosomal dominant Larsen syndrome (Orphanet:503)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dyggve-Melchior-Clausen disease (Orphanet:239)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
Geroderma osteodysplastica (Orphanet:2078)
Hurler syndrome (Orphanet:93473)
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis (Orphanet:93279)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
OSTEOGENESIS IMPERFECTA, TYPE VI (OMIM:613982)
Pseudoachondroplasia (Orphanet:750)
SMITH-MCCORT DYSPLASIA 1 (OMIM:607326)
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS (OMIM:609616)
Smith-McCort dysplasia (Orphanet:178355)
Stickler syndrome (Orphanet:828)