AREDYLD syndrome
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(Orphanet:1133)
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Cerebellar ataxia - hypogonadism
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(Orphanet:1173)
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Cortisone reductase deficiency 1
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(OMIM:604931)
|
Cushing disease
|
(Orphanet:96253)
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Familial partial lipodystrophy associated with PLIN1 mutations
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(Orphanet:280356)
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Familial partial lipodystrophy associated with PPARG mutations
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(Orphanet:79083)
|
GORDON HOLMES SYNDROME
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(OMIM:212840)
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HYPERPROLACTINEMIA
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(OMIM:615555)
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Hyperandrogenism due to cortisone reductase deficiency
|
(Orphanet:168588)
|
POLYCYSTIC OVARY SYNDROME 1
|
(OMIM:184700)
|
Perrault Syndrome 4
|
(OMIM:615300)
|
Prader-Willi syndrome
|
(Orphanet:739)
|
Wolfram syndrome 2
|
(OMIM:604928)
|