Cure My Disease

Don't miss your cure!

Log in / Sign up

Hereditary lethal multiple congenital anomalies/dysmorphic syndrome

MONDO:0043009

An 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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Disorder of development or morphogenesis (5188)

Sub-types of Hereditary lethal multiple congenital anomalies/dysmorphic syndrome

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
Bartsocas-Papas syndrome 1 0 trials
Edinburgh malformation syndrome 0 trials
Stromme syndrome 0 trials
Thakker-Donnai syndrome 0 trials
Endocrine-cerebro-osteodysplasia syndrome 0 trials
Lethal hydranencephaly-diaphragmatic hernia syndrome 0 trials
Lethal polymalformative syndrome, Boissel type 0 trials
Microphthalmia microtia fetal akinesia 0 trials
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome 0 trials

Including sub-types (1) Tagged with Hereditary lethal multiple congenital anomalies/dysmorphic syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.