Meckel syndrome
MONDO:0018921A rare, lethal, genetic, multiple congenital anomaly disorder characterized by the triad of brain malformation mainly occipital encephalocele, large polycystic kidneys, and polydactyly as well as associated abnormalities that may include cleft lip/palate, cardiac and genital anomalies, central nervous system (CNS) malformations, liver fibrosis, and bone dysplasia.
Also known as: Meckel-Gruber syndrome
3 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Meckel syndrome, type 1
(1)
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
(0)
Meckel syndrome 13
(0)
Meckel syndrome 14
(0)
Meckel syndrome, type 10
(0)
Meckel syndrome, type 11
(0)
Meckel syndrome, type 2
(0)
Meckel syndrome, type 3
(0)
Meckel syndrome, type 4
(0)
Meckel syndrome, type 5
(0)
Meckel syndrome, type 6
(0)
Meckel syndrome, type 8
(0)
Meckel syndrome, type 9
(0)
NPHP3-related Meckel-like syndrome
(0)
Broader categories
Disease
(618)
Hereditary disease
(172)
Syndromic disease
(24)
Human disease
(14)
Ciliopathy
(2)
Disease by molecular mechanism
(2)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)