Fetal akinesia deformation sequence 2
MONDO:0100102Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the RAPSN gene.
Also known as: FADS2
10 clinical trials for this condition and its sub-types.
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Disease
(618)
Hereditary disease
(172)
Respiratory system disorder
(127)
Syndromic disease
(24)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Congenital limb malformation
(3)
Disease of genetic or genomic mechanism
(2)
Arthrogryposis multiplex congenita
(1)
Multiple congenital anomalies/dysmorphic syndrome
(1)