Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome

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Subtype of: Spondyloepimetaphyseal dysplasia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
MONDO_0010077
DDR2 Causal
19110212 20223752 26463668 8434618
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome.
5 View disease cluster →
Warburg-cinotti syndrome 1 shared geneDDR2 Related via 1 shared gene including DDR2. Spondylometaepiphyseal dysplasia, short limb-hand type 1 shared geneDDR2 Related via 1 shared gene including DDR2. Choroidal melanoma 1 shared geneDDR2 Related via 1 shared gene including DDR2. Mesonephric adenocarcinoma 1 shared geneDDR2 Related via 1 shared gene including DDR2. Ganglioneuroblastoma 1 shared geneDDR2 Related via 1 shared gene including DDR2.