Craniofacial neurological cardiovascular and skeletal features (turnpenny-fry syndrome)

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Subtype of: Turnpenny-fry syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
craniofacial neurological cardiovascular and skeletal features (Turnpenny-Fry syndrome)
MONDO_0032707
PCGF2 Unknown
30343942 30526864 34750959 36105049
Open Targets
PCGF2-related craniofacial neurological cardiovascular and skeletal features (Turnpenny-Fry syndrome)
MONDO_0032707
PCGF2 Unknown
30526864 34750959 30343942 36105049
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Craniofacial neurological cardiovascular and skeletal features (turnpenny-fry syndrome).
5 View disease cluster →
Abnormality of the cerebrum 1 shared genePCGF2 Related via 1 shared gene including PCGF2. Turnpenny-fry syndrome 1 shared genePCGF2 Related via 1 shared gene including PCGF2. Abnormality of the skeletal system 1 shared genePCGF2 Related via 1 shared gene including PCGF2. Abnormality of the cardiovascular system 1 shared genePCGF2 Related via 1 shared gene including PCGF2. Wolfram syndrome 1 shared genePCGF2 Related via 1 shared gene including PCGF2.