Hydrolethalus syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
HYDROLETHALUS
2189
HYLS1 Unknown
15843405 18648327
Orphanet —
KIF7 Unknown
21552264
Orphanet
HYDROLETHALUS SYNDROME
C2931104MONDO:0006037MESH:C536079
HYLS1 Unknown
15843405 19656802 32509774 34212369 40009365
ClinGen, Disgenet, GWAS catalog —
KIF7 Unknown
21552264
CTD, Disgenet
PUS3 Unknown — Disgenet
HYDROLETHALUS SYNDROME 1
236680C1856016MESH:C565504MONDO:0009365
HYLS1 Unknown
15843405
CTD, ClinVar, Disgenet, GWAS catalog, HPO, ClinGen —
KIF7 Unknown — CTD, Disgenet
PUS3 Unknown — Disgenet
HYDROLETHALUS SYNDROME 2
614120C3279899MONDO:0013585
KIF7 Causal
19666503 21552264
CTD, ClinVar, Disgenet, HPO
All3 Causal1 Unknown3
Related Diseases Diseases that share the most curated genes with Hydrolethalus syndrome.
5 View disease cluster →
Acrocallosal syndrome 1 shared geneKIF7 Related via 1 shared gene including KIF7. Anencephaly 2 shared genesHYLS1, PUS3 Related via 2 shared genes including HYLS1, PUS3. Male infertility testicular dysgenesis 1 shared geneKIF7 Related via 1 shared gene including KIF7. Dandy-walker syndrome 2 shared genesHYLS1, PUS3 Related via 2 shared genes including HYLS1, PUS3. Cerebellar atrophy 2 shared genesHYLS1, PUS3 Related via 2 shared genes including HYLS1, PUS3.