Hypoplasia of the odontoid process
Symptom Information:
Symptom ID: | HPO:0003311 | ||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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: |
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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) |