Holoprosencephaly 13, x-linked

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Subtype of: Holoprosencephaly
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Holoprosencephaly 13, X-linked
MONDO_0019757
STAG2 Causal
29263825 33014403 28296084 30158690 31334757 37010288
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Holoprosencephaly 13, x-linked.
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Chromosome xq25 duplication syndrome 1 shared geneSTAG2 Related via 1 shared gene including STAG2. Xq25 microduplication syndrome 1 shared geneSTAG2 Related via 1 shared gene including STAG2. Developmental delay with microcephaly and congenital anomalies 1 shared geneSTAG2 Related via 1 shared gene including STAG2. Mullegama-klein-martinez syndrome 1 shared geneSTAG2 Related via 1 shared gene including STAG2. Growth delay 1 shared geneSTAG2 Related via 1 shared gene including STAG2.