Hypertrichosis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
HYPERTRICHOSIS
C0020555
ARID1B Causal — Disgenet
KCNJ11 Causal — Disgenet
HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA CANTU TYPE
MONDO:0009406
ABCC9 Causal
30089727 33529173 22610116 31175705 22608503 31828977 34453476
ClinGen, ClinVar, GWAS catalog
KCNJ8 Causal
24176758 24700710
CTD
All11 Causal4 Unknown8
Related Diseases Diseases that share the most curated genes with Hypertrichosis.
5 View disease cluster →
Cantu syndrome 2 shared genesABCC9, KCNJ8 Related via 2 shared genes including ABCC9, KCNJ8. Rubinstein-taybi syndrome 2 shared genesCREBBP, ASXL1 Related via 2 shared genes including CREBBP, ASXL1. X-linked congenital generalized hypertrichosis 1 shared geneSOX3 Related via 1 shared gene including SOX3. SOX3-related X-linked pituitary hormone deficiency with or without intellectual developmental disorder 1 shared geneSOX3 Related via 1 shared gene including SOX3. Acromegaloid facial appearance syndrome 1 shared geneABCC9 Related via 1 shared gene including ABCC9.