Autosomal dominant Robinow syndrome
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(Orphanet:3107)
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Autosomal recessive Robinow syndrome
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(Orphanet:1507)
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Autosomal recessive facio-digito-genital syndrome
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(Orphanet:1974)
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Baraitser-Winter syndrome
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(Orphanet:2995)
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Blepharo-cheilo-odontic syndrome
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(Orphanet:1997)
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Cardiofaciocutaneous syndrome
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(Orphanet:1340)
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Caudal appendage - deafness
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(Orphanet:1123)
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Craniosynostosis, Philadelphia type
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(Orphanet:1527)
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Dysmorphism - multiple structural anomalies
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(Orphanet:1780)
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Familial intestinal malrotation - facial anomalies
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(Orphanet:2454)
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Hypertrichosis
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(Orphanet:79365)
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Short stature - heart defect - craniofacial anomalies
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(Orphanet:1088)
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