gnathodiaphyseal dysplasia
human disease
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gnathodiaphyseal dysplasia
Summary
gnathodiaphyseal dysplasia is a hereditary disorder[1].
Key Facts
- gnathodiaphyseal dysplasia's instance of is recorded as hereditary disorder[2].
- gnathodiaphyseal dysplasia's instance of is recorded as developmental defect during embryogenesis[3].
- gnathodiaphyseal dysplasia's instance of is recorded as rare disease[4].
- gnathodiaphyseal dysplasia's instance of is recorded as class of disease[5].
- gnathodiaphyseal dysplasia is a type of autosomal dominant disease[6].
- gnathodiaphyseal dysplasia is a type of osteochondrodysplasia[7].
- gnathodiaphyseal dysplasia is a type of primary bone dysplasia with disorganized development of skeletal components[8].
- gnathodiaphyseal dysplasia is a type of primary bone dysplasia with decreased bone density[9].
- gnathodiaphyseal dysplasia's genetic association is recorded as ANO5[10].
- gnathodiaphyseal dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111533[11].
- gnathodiaphyseal dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:0111533[12].
- gnathodiaphyseal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_53697[13].