Spondyloepimetaphyseal dysplasia with joint laxity, 2

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Subtype of: Spondyloepimetaphyseal dysplasia
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Spondyloepimetaphyseal dysplasia with joint laxity, 2
  • Spondyloepimetaphyseal dysplasia with joint laxity, type 2
MONDO_0011335
KIF22 Unknown
19277648 22152677 22152678
Open Targets
All1 Causal0 Unknown1
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Larsen syndrome 1 shared geneKIF22 Related via 1 shared gene including KIF22. Spondyloepimetaphyseal dysplasia 1 shared geneKIF22 Related via 1 shared gene including KIF22. Desbuquois syndrome 1 shared geneKIF22 Related via 1 shared gene including KIF22. Alzheimer disease 1 shared geneKIF22 Related via 1 shared gene including KIF22.