BROWN-VIALETTO-VAN LAERE SYNDROME 1
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(OMIM:211530)
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Distal hereditary motor neuropathy type 7
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(Orphanet:139589)
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FEINGOLD SYNDROME 1
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(OMIM:164280)
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Feingold syndrome
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(Orphanet:1305)
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Hereditary neuropathy with liability to pressure palsies
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(Orphanet:640)
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Laryngeal abductor paralysis
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(Orphanet:2808)
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NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB
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(OMIM:607641)
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PARAGANGLIOMAS 1
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(OMIM:168000)
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PARAGANGLIOMAS 2
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(OMIM:601650)
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PARAGANGLIOMAS 3
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(OMIM:605373)
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Ptosis - vocal cord paralysis
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(Orphanet:2997)
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Riboflavin transporter deficiency
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(Orphanet:97229)
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Williams syndrome
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(Orphanet:904)
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