Hereditary lethal multiple congenital anomalies/dysmorphic syndrome
MONDO:0043009An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.
Also known as: genetic lethal multiple congenital anomalies/dysmorphic syndrome
1 clinical trial for this condition and its sub-types, 0 tagged with Hereditary lethal multiple congenital anomalies/dysmorphic syndrome itself.
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Browse by category →Sub-types of Hereditary lethal multiple congenital anomalies/dysmorphic syndrome
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Meckel syndrome 0 trials · 1 incl. sub-types
14 sub-types
- Meckel syndrome, type 1 1 trial
- Meckel syndrome 13 0 trials
- Meckel syndrome, type 10 0 trials
- Meckel syndrome, type 11 0 trials
- Meckel syndrome, type 2 0 trials
- Meckel syndrome, type 3 0 trials
- Meckel syndrome, type 4 0 trials
- Meckel syndrome, type 5 0 trials
- Meckel syndrome, type 6 0 trials
- Meckel syndrome, type 8 0 trials
- Meckel syndrome, type 9 0 trials
- NPHP3-related Meckel-like syndrome 0 trials
- Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome 0 trials
- Meckel syndrome 14 0 trials
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Bartsocas-Papas syndrome 1 0 trials
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Edinburgh malformation syndrome 0 trials
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Stromme syndrome 0 trials
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Thakker-Donnai syndrome 0 trials
Including sub-types (1)
Tagged with Hereditary lethal multiple congenital anomalies/dysmorphic syndrome (0)
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