Immunodeficiency-centromeric instability-facial anomalies syndrome 3
MONDO:0014828Any immunodeficiency-centromeric instability-facial anomalies syndrome in which the cause of the disease is a mutation in the CDCA7 gene.
Also known as: CDCA7 immunodeficiency-centromeric instability-facial anomalies syndrome, immunodeficiency-centromeric instability-Facial anomalies syndrome 3, immunodeficiency-centromeric instability-Facial anomalies syndrome type 3, immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in CDCA7, immunodeficiency-centromeric instability-facial anomalies syndrome type 3, ICF3, immunodeficiency-centromeric instability-FACIAL anomalies syndrome 3
3 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)
Telomere syndrome
(9)
Premature aging syndrome
(6)
Autosomal recessive disease
(4)
Disease of genetic or genomic mechanism
(2)
Immunodeficiency-centromeric instability-facial anomalies syndrome
(1)
Autosomal genetic disease
(0)
Disease by developmental or physiological process
(0)