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Orphanet classification of rare developmental anomalies during embryogenesis

Rare developmental defect during embryogenesis ORPHA:93890
- Multiple congenital anomalies/dysmorphic syndrome ORPHA:68341
  - Lethal multiple congenital anomalies/dysmorphic syndrome ORPHA:459787
    - Aprosencephaly/atelencephaly spectrum ORPHA:566847
    - Bartsocas-Papas syndrome ORPHA:1234
    - Diaphragmatic hernia-short bowel-asplenia syndrome ORPHA:527468
    - Diprosopus ORPHA:1681
    - Edinburgh malformation syndrome ORPHA:1895
    - Endocrine-cerebro-osteodysplasia syndrome ORPHA:199332
    - German syndrome ORPHA:2077
    - Lethal brain and heart developmental defects ORPHA:580933
    - Lethal faciocardiomelic dysplasia ORPHA:1972
    - Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome ORPHA:444069
    - Lethal hydranencephaly-diaphragmatic hernia syndrome ORPHA:480528
    - Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome ORPHA:2570
    - Lethal multiple pterygium syndrome ORPHA:33108
    - Lethal polymalformative syndrome, Boissel type ORPHA:210144
    - Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome ORPHA:615954
    - Macrosomia-microphthalmia-cleft palate syndrome ORPHA:2432
    - Meckel syndrome ORPHA:564
    - Microphthalmia-microtia-fetal akinesia syndrome ORPHA:2547
    - Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome ORPHA:500135
    - PAICS deficiency ORPHA:633099
    - Thakker-Donnai syndrome ORPHA:1780
    - Triploidy ORPHA:3376

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