Kenny-caffey syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
AUTOSOMAL DOMINANT KENNY-CAFFEY SYNDROME
93325C5681457MONDO:0007478
FAM111A Causal
23684011
ClinVar, Disgenet, GWAS catalog, Orphanet —
AUTOSOMAL RECESSIVE KENNY-CAFFEY SYNDROME
93324MONDO:0009486
TBCE Causal
12389028
ClinVar, GenCC, Orphanet —
All3 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Kenny-caffey syndrome.
5 View disease cluster →
Osteocraniostenosis 1 shared geneFAM111A Related via 1 shared gene including FAM111A. FAM111A-related skeletal dysplasia 1 shared geneFAM111A Related via 1 shared gene including FAM111A. Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE. Sanjad-sakati syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE. encephalopathy, progressive, with amyotrophy and optic atrophy 1 shared geneTBCE Related via 1 shared gene including TBCE.