Wilson-turner syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WILSON-TURNER SYNDROME
3459MONDO:0010665
LAS1L Causal — CTD, ClinVar, Orphanet
HDAC8 Unknown — CTD, Orphanet
WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME
MESH:C536708
LAS1L Unknown
26358559 25644381
CTD
All2 Causal1 Unknown2
Related Diseases Diseases that share the most curated genes with Wilson-turner syndrome.
5 View disease cluster →
De lange syndrome 1 shared geneHDAC8 Related via 1 shared gene including HDAC8. X-linked syndromic intellectual disability 1 shared geneLAS1L Related via 1 shared gene including LAS1L. Cornelia de lange syndrome 1 shared geneHDAC8 Related via 1 shared gene including HDAC8. Partington syndrome 1 shared geneLAS1L Related via 1 shared gene including LAS1L. Clinodactyly 1 shared geneHDAC8 Related via 1 shared gene including HDAC8.