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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
1 clinical trial for this condition and its sub-types, 0 tagged with Meckel syndrome itself.
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Sub-types of Meckel syndrome
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Meckel syndrome, type 1 1 trial
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Meckel syndrome 13 0 trials
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Meckel syndrome, type 10 0 trials
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Meckel syndrome, type 11 0 trials
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Meckel syndrome, type 2 0 trials
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Meckel syndrome, type 3 0 trials
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Meckel syndrome, type 4 0 trials
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Meckel syndrome, type 5 0 trials
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Meckel syndrome, type 6 0 trials
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Meckel syndrome, type 8 0 trials
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Meckel syndrome, type 9 0 trials
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NPHP3-related Meckel-like syndrome 0 trials
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Meckel syndrome 14 0 trials