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Noonan syndrome-like disorder with loose anagen hair
Noonan syndrome-like disorder with loose anagen hair
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Noonan syndrome-like disorder with loose anagen hair
PPP1CB
Causal
—
ClinGen
mRNA surveillance pathway
cGMP-PKG signaling pathway
cAMP signaling pathway
Oocyte meiosis
Cellular senescence
Adrenergic signaling in cardiomyocytes
Vascular smooth muscle contraction
Hippo signaling pathway
Focal adhesion
Platelet activation
Long-term potentiation
Dopaminergic synapse
Inflammatory mediator regulation of TRP channels
Regulation of actin cytoskeleton
Insulin signaling pathway
Oxytocin signaling pathway
Insulin resistance
Amphetamine addiction
Alcoholism
Herpes simplex virus 1 infection
Proteoglycans in cancer
Diabetic cardiomyopathy
Regulation of PLK1 Activity at G2/M Transition
RHO GTPases activate PKNs
RHO GTPases activate PAKs
+22 more
SHOC2
Causal
—
ClinGen
Ras signaling pathway
All
2
Causal
2
Unknown
0
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
2
Related Diseases
Diseases that share the most curated genes with Noonan syndrome-like disorder with loose anagen hair.
5
View disease cluster →
Cardiofaciocutaneous syndrome
1 shared gene
SHOC2
Related via 1 shared gene including SHOC2.
Costello syndrome
1 shared gene
SHOC2
Related via 1 shared gene including SHOC2.
Noonan syndrome
2 shared genes
SHOC2, PPP1CB
Related via 2 shared genes including SHOC2, PPP1CB.
Dandy-walker syndrome
1 shared gene
PPP1CB
Related via 1 shared gene including PPP1CB.
Non-immune hydrops fetalis
1 shared gene
SHOC2
Related via 1 shared gene including SHOC2.
1
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