spondyloepimetaphyseal dysplasia, Strudwick type
Human disease
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spondyloepimetaphyseal dysplasia, Strudwick type
Summary
spondyloepimetaphyseal dysplasia, Strudwick type is a developmental defect during embryogenesis[1].
Key Facts
- spondyloepimetaphyseal dysplasia, Strudwick type's instance of is recorded as developmental defect during embryogenesis[2].
- spondyloepimetaphyseal dysplasia, Strudwick type's instance of is recorded as rare disease[3].
- spondyloepimetaphyseal dysplasia, Strudwick type's instance of is recorded as class of disease[4].
- spondyloepimetaphyseal dysplasia, Strudwick type is a type of spondyloepimetaphyseal dysplasia[5].
- spondyloepimetaphyseal dysplasia, Strudwick type is a type of type 2 collagen-related bone disorder[6].
- spondyloepimetaphyseal dysplasia, Strudwick type is a type of autosomal dominant disease[7].
- spondyloepimetaphyseal dysplasia, Strudwick type's symptoms and signs is recorded as short stature[8].
- spondyloepimetaphyseal dysplasia, Strudwick type's ICD-9-CM is recorded as 758.89[9].
- spondyloepimetaphyseal dysplasia, Strudwick type's genetic association is recorded as COL2A1[10].
- spondyloepimetaphyseal dysplasia, Strudwick type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080028[11].
- spondyloepimetaphyseal dysplasia, Strudwick type's exact match is recorded as http://identifiers.org/doid/DOID:0080028[12].
- spondyloepimetaphyseal dysplasia, Strudwick type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_93346[13].
- spondyloepimetaphyseal dysplasia, Strudwick type's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- spondyloepimetaphyseal dysplasia, Strudwick type's has phenotype is recorded as clubfoot[15].
- spondyloepimetaphyseal dysplasia, Strudwick type's has phenotype is recorded as scoliosis[16].
- spondyloepimetaphyseal dysplasia, Strudwick type's has phenotype is recorded as pectus carinatum[17].
- spondyloepimetaphyseal dysplasia, Strudwick type's has phenotype is recorded as abnormal lordosis[18].
- spondyloepimetaphyseal dysplasia, Strudwick type's has phenotype is recorded as coxa vara[19].