Cleidocranial dysplasia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CLEIDOCRANIAL DYSOSTOSIS
RUNX2 Causal — ClinVar
CLEIDOCRANIAL DYSPLASIA
1452C0008928MESH:D002973
RUNX2 Unknown
14688224 17022082 20357738
CTD, Disgenet, Orphanet
SUPT3H Unknown — Disgenet
CLEIDOCRANIAL DYSPLASIA 1
119600MONDO:0007340
RUNX2 Unknown
9182765 9207800 10545612 10521292 15952089 12424590 12081718
GWAS catalog, HPO
CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, DENTAL ANOMALIES ONLY
C5774315
RUNX2 Causal — Disgenet
CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, WITH BRACHYDACTYLY
C5774312
RUNX2 Causal
10521292 10545612 12081718 12424590 15952089 9182765 9207800
Disgenet
CLEIDOCRANIAL DYSPLASIA 2
620099C5774243MONDO:0859307
CBFB Causal
36241386
ClinVar, Disgenet, GWAS catalog, HPO, ClinGen
All3 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Cleidocranial dysplasia.
5 View disease cluster →
Metaphyseal dysplasia 1 shared geneRUNX2 Related via 1 shared gene including RUNX2. Facial nerve disorder 1 shared geneSUPT3H Related via 1 shared gene including SUPT3H. Tooth abnormalities 1 shared geneRUNX2 Related via 1 shared gene including RUNX2. Diffuse idiopathic skeletal hyperostosis 1 shared geneSUPT3H Related via 1 shared gene including SUPT3H. Uremia 1 shared geneRUNX2 Related via 1 shared gene including RUNX2.