Craniofacial deafness hand syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CRANIOFACIAL DEAFNESS HAND SYNDROME
C1852510MESH:C536453
PAX3 Unknown
18553554
CTD, Disgenet
CRANIOFACIAL-DEAFNESS-HAND SYNDROME
1228801529MONDO:0007395
PAX3 Causal
6859126 8664898
ClinVar, GenCC, HPO, Orphanet
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Craniofacial deafness hand syndrome.
5 View disease cluster →
Kleins syndrome 1 shared genePAX3 Related via 1 shared gene including PAX3. Congenital hand deformities 1 shared genePAX3 Related via 1 shared gene including PAX3. Central precocious puberty 1 shared genePAX3 Related via 1 shared gene including PAX3. Waardenburg syndrome 1 shared genePAX3 Related via 1 shared gene including PAX3. Congenital diaphragmatic hernia 1 shared genePAX3 Related via 1 shared gene including PAX3.