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Orphanet classification of rare developmental anomalies during embryogenesis

Rare developmental defect during embryogenesis ORPHA:93890
- Branchial arch or oral-acral syndrome ORPHA:139036
- Central nervous system malformation ORPHA:98044
- Congenital limb malformation ORPHA:68378
- Conjoined twins ORPHA:647916
- Cranial malformation ORPHA:98038
- Developmental anomaly of metabolic origin ORPHA:139009
- Developmental defect of the eye ORPHA:98553
- Diaphragmatic or abdominal wall malformation ORPHA:98043
- Difference of sex development ORPHA:90771
- Digestive tract malformation ORPHA:98039
- Hydrops fetalis ORPHA:1041
- Malformation syndrome with hamartosis ORPHA:98196
- Malformation syndrome with odontal and/or periodontal component ORPHA:139042
- Malformation syndrome with short stature ORPHA:139021
- Multiple congenital anomalies/dysmorphic syndrome ORPHA:68341
- Overgrowth/obesity syndrome ORPHA:139024
- Progeroid syndrome ORPHA:139033
- Rare bone development disorder ORPHA:139012
- Rare chromosomal anomaly ORPHA:68335
- Rare developmental defect with connective tissue involvement ORPHA:139030
- Rare developmental defect with skin/mucosae involvement ORPHA:139027
- Rare head and neck malformation ORPHA:155832
- Rare surgical cardiac disease ORPHA:97965
- Rare teratologic disease ORPHA:52662
- Renal or urinary tract malformation ORPHA:93545
- Respiratory or mediastinal malformation ORPHA:98045
- Syndromic genetic deafness ORPHA:90642
- Urogenital tract malformation ORPHA:83001
- Vascular anomaly or angioma ORPHA:68419
- Visceral malformation of the liver, biliary tract, pancreas or spleen ORPHA:98041

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