Wiedemann-steiner syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WIEDEMANN STEINER SYNDROME
C1854630
ARID1B Unknown
26739615
Disgenet
CHD7 Unknown
26056227
Disgenet —
KMT2A Unknown
23623388
Disgenet
SMC1A Unknown — Disgenet
SMC3 Unknown — Disgenet
WIEDEMANN-STEINER SYNDROME
319182605130MONDO:0011518OMIM:605130
KMT2A Causal
22795537 24818805 24886118 25810209 25929198 27320412 27759909 27777327 28815892 29203834 30549396 30841869 31044088 31168168 31250358 32311999 33043602 34469078
CTD, ClinGen, ClinVar, Disgenet, HPO, Orphanet
All5 Causal1 Unknown5
Related Diseases Diseases that share the most curated genes with Wiedemann-steiner syndrome.
5 View disease cluster →
Cornelia de lange syndrome 3 shared genesKMT2A, SMC1A, SMC3 Related via 3 shared genes including KMT2A, SMC1A, SMC3. De lange syndrome 2 shared genesSMC1A, SMC3 Related via 2 shared genes including SMC1A, SMC3. Congenital muscular hypertrophy-cerebral syndrome 1 shared geneSMC1A Related via 1 shared gene including SMC1A. Craniofacial ulnar renal syndrome 1 shared geneCHD7 Related via 1 shared gene including CHD7. Choanal atresia syndrome 1 shared geneCHD7 Related via 1 shared gene including CHD7.