Hypoplasia of the odontoid process

Symptom Information:

Symptom ID: HPO:0003311
Synonyms:
Hypoplastic odontoid process [HPO:0003311]
Odontoid hypoplasia [HPO:0003311]
Small odontoid process [HPO:0003311]
Odontoid process hypoplasia [Orphanet:16330]
Hypoplastic odontoid process [OMIM:Hypoplastic odontoid process]
Odontoid hypoplasia [OMIM:Odontoid hypoplasia]
Small odontoid process [OMIM:Small odontoid process]
Odontoid hypoplasia [Orphanet:16330]
Odontoid (dens) hypoplasia [OMIM:Odontoid (dens) hypoplasia]
Odontoid process hypoplasia [OMIM:Odontoid process hypoplasia]
Quality:
Cross references:
Orphanet:16330 "Odontoid hypoplasia" [Orphanet:16330]
OMIM: "Hypoplastic odontoid process" [OMIM:Hypoplastic odontoid process]
OMIM: "Odontoid hypoplasia" [OMIM:Odontoid hypoplasia]
OMIM: "Small odontoid process" [OMIM:Small odontoid process]
OMIM: "Odontoid (dens) hypoplasia" [OMIM:Odontoid (dens) hypoplasia]
OMIM: "Odontoid process hypoplasia" [OMIM:Odontoid process hypoplasia]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia involving the vertebral column
HPO         Abnormality of the odontoid process
Orphanet 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)
             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)
                      Hypoplasia of the odontoid process(HPO:0003311)
             Abnormal axial skeleton morphology(HPO:0009121)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Hypoplasia of the odontoid process(HPO:0003311)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the odontoid process(HPO:0003310)
                      Hypoplasia of the odontoid process(HPO:0003311)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Hypoplasia of the odontoid process(HPO:0003311)
MedDRA:
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

AARSKOG-SCOTT SYNDROME (OMIM:305400)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
CODAS syndrome (Orphanet:1458)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Fucosidosis (Orphanet:349)
Hurler syndrome (Orphanet:93473)
MORQUIO SYNDROME C (OMIM:252300)
Marshall-Smith syndrome (Orphanet:561)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
ODONTOID HYPOPLASIA (OMIM:613628)
Pseudoachondroplasia (Orphanet:750)
Pseudodiastrophic dysplasia (Orphanet:85174)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
SMITH-MCCORT DYSPLASIA 1 (OMIM:607326)
SMITH-MCCORT DYSPLASIA 2 (OMIM:615222)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT (OMIM:184100)
Smith-McCort dysplasia (Orphanet:178355)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Orphanet:93358)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)