Achondrogenesis type 1B
|
(Orphanet:93298)
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Achondrogenesis type 2
|
(Orphanet:93296)
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BARTTER SYNDROME, TYPE 4A
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(OMIM:602522)
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BARTTER SYNDROME, TYPE 4B
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(OMIM:613090)
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CARDIAC VALVULAR DEFECT, DEVELOPMENTAL
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(OMIM:212093)
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Cervicofacial lymphatic malformation
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(Orphanet:137923)
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Cystic hygroma
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(Orphanet:79486)
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Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form
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(Orphanet:308712)
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Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
|
(Orphanet:308684)
|
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
|
(Orphanet:308698)
|
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
|
(Orphanet:308670)
|
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
|
(Orphanet:308655)
|
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
|
(Orphanet:308638)
|
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
|
(Orphanet:308621)
|
Hypochondrogenesis
|
(Orphanet:93297)
|