2p21 microdeletion syndrome
|
(Orphanet:163693)
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Atypical hypotonia - cystinuria syndrome
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(Orphanet:238523)
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CK syndrome
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(Orphanet:251383)
|
Cohen syndrome
|
(Orphanet:193)
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FANCONI ANEMIA, COMPLEMENTATION GROUP P
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(OMIM:613951)
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Hypotonia - cystinuria syndrome
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(Orphanet:163690)
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Intellectual deficit, X-linked, Brooks type
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(Orphanet:3056)
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Intellectual deficit, X-linked, Nascimento type
|
(Orphanet:163956)
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MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE
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(OMIM:612947)
|
PALANT CLEFT PALATE SYNDROME
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(OMIM:260150)
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Prader-Willi syndrome
|
(Orphanet:739)
|
SCHAAF-YANG SYNDROME
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(OMIM:615547)
|