Coronal cleft vertebrae

Symptom Information:

Symptom ID: HPO:0003417
Synonyms:
coronal cleft of vertebrae [HPO:0003417]
Coronal clefts [HPO:0003417]
Coronal vertebral clefts [HPO:0003417]
Vertebral coronal clefts [HPO:0003417]
Coronal cleft of vertebrae [OMIM:Coronal cleft of vertebrae]
Coronal cleft vertebrae [OMIM:Coronal cleft vertebrae]
Coronal clefts [OMIM:Coronal clefts]
Coronal vertebral clefts [OMIM:Coronal vertebral clefts]
Vertebral coronal clefts [OMIM:Vertebral coronal clefts]
Coronal cleft [OMIM:Coronal cleft]
Coronal clefts (neonate) [OMIM:Coronal clefts (neonate)]
Vertebral coronal clefts (T11-S2) [OMIM:Vertebral coronal clefts (T11-S2)]
Vertebral coronal clefts (newborn) [OMIM:Vertebral coronal clefts (newborn)]
Quality:
Cross references:
OMIM: "Coronal cleft of vertebrae" [OMIM:Coronal cleft of vertebrae]
OMIM: "Coronal cleft vertebrae" [OMIM:Coronal cleft vertebrae]
OMIM: "Coronal clefts" [OMIM:Coronal clefts]
OMIM: "Coronal vertebral clefts" [OMIM:Coronal vertebral clefts]
OMIM: "Vertebral coronal clefts" [OMIM:Vertebral coronal clefts]
OMIM: "Coronal cleft" [OMIM:Coronal cleft]
OMIM: "Coronal clefts (neonate)" [OMIM:Coronal clefts (neonate)]
OMIM: "Vertebral coronal clefts (T11-S2)" [OMIM:Vertebral coronal clefts (T11-S2)]
OMIM: "Vertebral coronal clefts (newborn)" [OMIM:Vertebral coronal clefts (newborn)]
Is a (Direct Parents):
HPO         Vertebral clefting
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)
                         Vertebral clefting(HPO:0008428)
                            Coronal cleft vertebrae(HPO:0003417)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Atelosteogenesis type I (Orphanet:1190)
Atelosteogenesis type II (Orphanet:56304)
CHST3-related skeletal dysplasia (Orphanet:263463)
CODAS syndrome (Orphanet:1458)
Chondrodysplasia punctata, tibial-metacarpal type (Orphanet:79346)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
Goldblatt syndrome (Orphanet:166272)
Kniest dysplasia (Orphanet:485)
Lethal Kniest-like dysplasia (Orphanet:2347)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
Rhizomelic chondrodysplasia punctata (Orphanet:177)
Rhizomelic chondrodysplasia punctata type 1 (Orphanet:309789)
Schwartz-Jampel syndrome (Orphanet:800)
Weissenbacher- Zweymuller syndrome (Orphanet:3450)