osteoglophonic dwarfism
Osteoglophonic dwarfism (OGD) is characterized by dwarfism, severe craniofacial abnormalities and multiple unerupted teeth
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osteoglophonic dwarfism
Summary
osteoglophonic dwarfism is a developmental defect during embryogenesis[1].
Key Facts
- osteoglophonic dwarfism's instance of is recorded as developmental defect during embryogenesis[2].
- osteoglophonic dwarfism's instance of is recorded as rare disease[3].
- osteoglophonic dwarfism's instance of is recorded as class of disease[4].
- osteoglophonic dwarfism is a type of primary bone dysplasia with disorganized development of skeletal components[5].
- osteoglophonic dwarfism is a type of autosomal dominant disease[6].
- osteoglophonic dwarfism is a type of osteochondrodysplasia[7].
- osteoglophonic dwarfism's genetic association is recorded as FGFR1[8].
- osteoglophonic dwarfism's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2645[9].
- osteoglophonic dwarfism's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111532[10].
- osteoglophonic dwarfism's exact match is recorded as http://identifiers.org/doid/DOID:0111532[11].