Central precocious puberty

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CENTRAL PRECOCIOUS PUBERTY
C0342543
DLK1 Causal — Disgenet —
CENTRAL PRECOCIOUS PUBERTY 1
MONDO:0008302
KISS1R Causal — ClinVar, GenCC
All11 Causal2 Unknown9
Related Diseases Diseases that share the most curated genes with Central precocious puberty.
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Vogt-koyanagi-harada disease 2 shared genesC1orf141, IL23R Related via 2 shared genes including C1orf141, IL23R. Craniofacial deafness hand syndrome 1 shared genePAX3 Related via 1 shared gene including PAX3. Temple syndrome 1 shared geneDLK1 Related via 1 shared gene including DLK1. Estrogen resistance 1 shared geneESR1 Related via 1 shared gene including ESR1. Kleins syndrome 1 shared genePAX3 Related via 1 shared gene including PAX3.