spondyloepiphyseal dysplasia, Maroteaux type
human disease
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spondyloepiphyseal dysplasia, Maroteaux type
Summary
spondyloepiphyseal dysplasia, Maroteaux type is a developmental defect during embryogenesis[1].
Key Facts
- spondyloepiphyseal dysplasia, Maroteaux type's instance of is recorded as developmental defect during embryogenesis[2].
- spondyloepiphyseal dysplasia, Maroteaux type's instance of is recorded as rare disease[3].
- spondyloepiphyseal dysplasia, Maroteaux type's instance of is recorded as class of disease[4].
- spondyloepiphyseal dysplasia, Maroteaux type is a type of TRPV4-related bone disorder[5].
- spondyloepiphyseal dysplasia, Maroteaux type is a type of spondyloepiphyseal dysplasia with congenital joint dislocations[6].
- spondyloepiphyseal dysplasia, Maroteaux type is a type of spondyloepiphyseal dysplasia[7].
- spondyloepiphyseal dysplasia, Maroteaux type is a type of autosomal dominant disease[8].
- spondyloepiphyseal dysplasia, Maroteaux type is a type of osteochondrodysplasia[9].
- spondyloepiphyseal dysplasia, Maroteaux type's genetic association is recorded as TRPV4[10].
- spondyloepiphyseal dysplasia, Maroteaux type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_263482[11].
- spondyloepiphyseal dysplasia, Maroteaux type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111553[12].
- spondyloepiphyseal dysplasia, Maroteaux type's exact match is recorded as http://identifiers.org/doid/DOID:0111553[13].