Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis (soft syndrome)

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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, onychodysplasia, facial dysmorphism, and hypotrichosis (SOFT syndrome)
MONDO_0013894
POC1A Unknown
22440536 22840363 22840364 26162852 26336158 26374189 26791357 28819016 33372278 35234134
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis (soft syndrome).
5 View disease cluster →
Soft syndrome 1 shared genePOC1A Related via 1 shared gene including POC1A. Type a insulin resistance syndrome 1 shared genePOC1A Related via 1 shared gene including POC1A. Dwarfism 1 shared genePOC1A Related via 1 shared gene including POC1A. Primary microcephaly 1 shared genePOC1A Related via 1 shared gene including POC1A. Pituitary dwarfism 1 shared genePOC1A Related via 1 shared gene including POC1A.