Hydrolethalus syndrome 2
MONDO:0013585Any hydrolethalus syndrome in which the cause of the disease is a mutation in the KIF7 gene.
Also known as: KIF7 hydrolethalus syndrome, hydrolethalus syndrome 2, hydrolethalus syndrome caused by mutation in KIF7, hydrolethalus syndrome type 2, HLS2
2 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Hereditary disease
(172)
Human disease
(14)
Autosomal recessive disease
(4)
Ciliopathy
(2)
Disease by molecular mechanism
(2)
Disease of genetic or genomic mechanism
(2)
Autosomal genetic disease
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)