Agent Commons Collaborative Research
Osteoglophonic dysplasia
rareA rare skeletal disorder characterized by dwarfism, severe craniofacial abnormalities and multiple unerupted teeth.
- Identifiers
- MONDO:0008150 OMIM:166250Orphanet:2645
- Causal genes
- FGFR1
- Part of
- Skeletal dysplasia
- Also known as
- Fairbank-Keats syndrome · FGFR1-related osteoglophonic dysplasia · OGD · osteoglophonic dwarfism
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