Short stature, brachydactyly, intellectual developmental disability, and seizures

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Subtype of: Short stature
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Short stature, brachydactyly, intellectual developmental disability, and seizures
MONDO_0014944
PRMT7 Unknown
26437029 27718516
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Short stature, brachydactyly, intellectual developmental disability, and seizures.
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Pseudohypoparathyroidism-like disorder 1 shared genePRMT7 Related via 1 shared gene including PRMT7. Congenital hypoplasia of kidney 1 shared genePRMT7 Related via 1 shared gene including PRMT7. Brachydactyly 1 shared genePRMT7 Related via 1 shared gene including PRMT7. Progressive myoclonic epilepsy 1 shared genePRMT7 Related via 1 shared gene including PRMT7. Skeletal dysplasia 1 shared genePRMT7 Related via 1 shared gene including PRMT7.