19q13.11 microdeletion syndrome
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(Orphanet:217346)
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3C syndrome
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(Orphanet:7)
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Congenital alveolar capillary dysplasia
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(Orphanet:210122)
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Congenital osteogenesis imperfecta - microcephaly - cataracts
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(Orphanet:2772)
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Diabetic embryopathy
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(Orphanet:1926)
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Emanuel syndrome
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(Orphanet:96170)
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Familial caudal dysgenesis
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(Orphanet:1768)
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Fibulo-ulnar hypoplasia - renal anomalies
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(Orphanet:2256)
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Holzgreve-Wagner-Rehder syndrome
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(Orphanet:2167)
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Lowry-MacLean syndrome
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(Orphanet:2409)
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MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
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(OMIM:615009)
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Meckel syndrome
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(Orphanet:564)
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Meckel syndrome, type 1
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(OMIM:249000)
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Mosaic trisomy 9
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(Orphanet:99776)
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Omphalocele syndrome, Shprintzen-Goldberg type
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(Orphanet:3164)
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Short rib-polydactyly syndrome, Beemer-Langer type
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(Orphanet:93268)
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Spondylocostal dysostosis - anal and genitourinary malformations
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(Orphanet:94095)
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Tetraamelia - multiple malformations
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(Orphanet:3301)
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Ulbright-Hodes syndrome
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(Orphanet:3404)
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Umbilical cord ulceration - intestinal atresia
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(Orphanet:3405)
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VACTERL with hydrocephalus
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(Orphanet:3412)
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VACTERL/VATER association
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(Orphanet:887)
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Van den Ende-Gupta syndrome
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(Orphanet:2460)
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