Prader-willi syndrome

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
PRADER-WILLI SYNDROME
176270C0032897MESH:D011218MONDO:0008300
HERC2 Causal — CTD, ClinVar, Disgenet, HPO
MAGEL2 Causal
24076603
CTD, ClinVar, Disgenet, HPO —
PRADER-WILLI-LIKE SYNDROME
C3809877
MAGEL2 Causal — Disgenet —
All8 Causal2 Unknown7
Related Diseases Diseases that share the most curated genes with Prader-willi syndrome.
5 View disease cluster →
Skin hair eye pigmentation variation 2 shared genesHERC2, OCA2 Related via 2 shared genes including HERC2, OCA2. Angelman syndrome 2 shared genesOCA2, SNRPN Related via 2 shared genes including OCA2, SNRPN. Developmental delay with autism spectrum disorder 1 shared geneHERC2 Related via 1 shared gene including HERC2. Schaaf-yang syndrome 1 shared geneMAGEL2 Related via 1 shared gene including MAGEL2. Brown oculocutaneous albinism 1 shared geneOCA2 Related via 1 shared gene including OCA2.