Atypical Mayer-Rokitansky-Küster-Hauser syndrome
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(Orphanet:247768)
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Bardet-Biedl syndrome 10
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(OMIM:615987)
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Blepharophimosis - epicanthus inversus - ptosis
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(Orphanet:126)
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Classic Mayer-Rokitansky-Küster-Hauser syndrome
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(Orphanet:247775)
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Fuhrmann syndrome
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(Orphanet:2854)
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HYMEN, IMPERFORATE
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(OMIM:237100)
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HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL
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(OMIM:145295)
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Hemochromatosis type 3
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(Orphanet:225123)
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Hemochromatosis, type 1
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(OMIM:235200)
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Hemochromatosis, type 2A
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(OMIM:602390)
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MELAS
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(Orphanet:550)
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POLYCYSTIC OVARY SYNDROME 1
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(OMIM:184700)
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PREMATURE OVARIAN FAILURE 9
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(OMIM:615724)
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Perrault Syndrome 2
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(OMIM:614926)
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Prader-Willi syndrome
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(Orphanet:739)
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SATOYOSHI SYNDROME
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(OMIM:600705)
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