Biconcave vertebral bodies

Symptom Information:

Symptom ID: HPO:0004586
Synonyms:
Biconcave 'codfish' vertebrae [HPO:0004586]
Biconcave vertebrae [HPO:0004586]
Codfish vertebrae [HPO:0004586]
Fish vertebrae [HPO:0004586]
Scalloping of vertebral bodies [HPO:0004586]
Biconcave 'codfish' vertebrae [OMIM:Biconcave 'codfish' vertebrae]
Biconcave vertebrae [OMIM:Biconcave vertebrae]
Biconcave vertebral bodies [OMIM:Biconcave vertebral bodies]
Codfish vertebrae [OMIM:Codfish vertebrae]
Scalloping of vertebral bodies [OMIM:Scalloping of vertebral bodies]
Biconcave vertebral bodies (later childhood) [OMIM:Biconcave vertebral bodies (later childhood)]
Quality:
Cross references:
OMIM: "Biconcave 'codfish' vertebrae" [OMIM:Biconcave 'codfish' vertebrae]
OMIM: "Biconcave vertebrae" [OMIM:Biconcave vertebrae]
OMIM: "Biconcave vertebral bodies" [OMIM:Biconcave vertebral bodies]
OMIM: "Codfish vertebrae" [OMIM:Codfish vertebrae]
OMIM: "Scalloping of vertebral bodies" [OMIM:Scalloping of vertebral bodies]
OMIM: "Biconcave vertebral bodies (later childhood)" [OMIM:Biconcave vertebral bodies (later 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)
                         Biconcave vertebral bodies(HPO:0004586)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Classical homocystinuria (Orphanet:394)
Cushing disease (Orphanet:96253)
Geroderma osteodysplastica (Orphanet:2078)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Lateral meningocele syndrome (Orphanet:2789)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Mucopolysaccharidosis type 1 (Orphanet:579)
OSTEOGENESIS IMPERFECTA, TYPE III (OMIM:259420)
OSTEOGENESIS IMPERFECTA, TYPE V (OMIM:610967)
OSTEOGENESIS IMPERFECTA, TYPE VI (OMIM:613982)
OSTEOGENESIS IMPERFECTA, TYPE XI (OMIM:610968)
Osteogenesis imperfecta type 3 (Orphanet:216812)
Osteogenesis imperfecta type 5 (Orphanet:216828)
RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA (OMIM:610319)
SPONASTRIME dysplasia (Orphanet:93357)