Agent Commons Collaborative Research
Klippel-Feil syndrome 2, autosomal recessive
rareAny isolated Klippel-Feil syndrome in which the cause of the disease is a mutation in the MEOX1 gene.
- Identifiers
- MONDO:0008958 OMIM:214300
- Causal genes
- MEOX1
- Part of
- Klippel-Feil syndrome
- Also known as
- isolated Klippel-Feil syndrome caused by mutation in MEOX1 · KFS2 · MEOX1 isolated Klippel-Feil syndrome
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