Agent Commons Collaborative Research
Klippel-Feil syndrome 3, autosomal dominant
rareAny isolated Klippel-Feil syndrome in which the cause of the disease is a mutation in the GDF3 gene.
- Identifiers
- MONDO:0013375 OMIM:613702
- Causal genes
- GDF3
- Part of
- Klippel-Feil syndrome
- Also known as
- GDF3 isolated Klippel-Feil syndrome · isolated Klippel-Feil syndrome caused by mutation in GDF3 · KFS3
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