15q24 microdeletion syndrome
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(Orphanet:94065)
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AARSKOG SYNDROME, AUTOSOMAL DOMINANT
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(OMIM:100050)
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AARSKOG-SCOTT SYNDROME
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(OMIM:305400)
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Aarskog-Scott syndrome
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(Orphanet:915)
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Acro-fronto-facio-nasal dysostosis
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(Orphanet:1784)
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Autosomal dominant Opitz G/BBB syndrome
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(Orphanet:306588)
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Autosomal recessive facio-digito-genital syndrome
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(Orphanet:1974)
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Brachymorphism - onychodysplasia - dysphalangism
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(Orphanet:1292)
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Craniofrontonasal dysplasia
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(Orphanet:1520)
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Cyprus facial-neuromusculoskeletal syndrome
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(Orphanet:2674)
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Deafness - enamel hypoplasia - nail defects
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(Orphanet:3220)
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Donnai-Barrow syndrome
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(Orphanet:2143)
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Frontonasal dysplasia
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(Orphanet:250)
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HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES
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(OMIM:614684)
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Hypertelorism - hypospadias - polysyndactyly syndrome
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(Orphanet:2211)
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Hypertelorism, Teebi type
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(Orphanet:1519)
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MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM
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(OMIM:606242)
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Macrocephaly - spastic paraplegia - dysmorphism
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(Orphanet:2429)
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Nasopalpebral lipoma - coloboma - telecanthus
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(Orphanet:2399)
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Opitz G/BBB syndrome
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(Orphanet:2745)
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Schilbach-Rott syndrome
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(Orphanet:2353)
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Trisomy 17p
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(Orphanet:261290)
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WIDOW'S PEAK
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(OMIM:194000)
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WIDOW'S PEAK SYNDROME
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(OMIM:314570)
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Wolf-Hirschhorn syndrome
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(Orphanet:280)
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X-linked Opitz G/BBB syndrome
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(Orphanet:306597)
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