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
C5681457
TBCE Unknown — Disgenet —
KENNY-CAFFEY SYNDROME, TYPE 1
C1855648244460MESH:C537021
B3GALNT2 Unknown — Disgenet
TBCE Unknown — CTD, Disgenet, HPO —
KENNY-CAFFEY SYNDROME, TYPE 2
127000C4316787MESH:C537020
FAM111A Unknown
23684011
CTD, Disgenet, HPO —
TBCE Unknown
12389028
CTD, Disgenet —
All3 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Kenny-caffey syndrome.
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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.