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choroidal dystrophy, central areolar 2
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MONDO:0013137 |
|
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macular dystrophy, progressive
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MONDO:0013137 |
|
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PRPH2 central areolar choroidal dystrophy
|
MONDO:0013137 |
|
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choroidal dystrophy, central areolar type 2
|
MONDO:0013137 |
|
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central areolar choroidal dystrophy caused by mutation in PRPH2
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MONDO:0013137 |
|
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vertigo, benign recurrent, 2
|
MONDO:0013138 |
|
|
neutropenia, severe congenital, 2, autosomal dominant
|
MONDO:0013139 |
|
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GFI1 autosomal dominant severe congenital neutropenia
|
MONDO:0013139 |
|
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neutropenia, severe congenital 2, autosomal dominant
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MONDO:0013139 |
|
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candidiasis, familial chronic mucocutaneous
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MONDO:0013140 |
|
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candidiasis, familial, 4, autosomal recessive
|
MONDO:0013140 |
|
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CLEC7A familial chronic mucocutaneous candidiasis
|
MONDO:0013140 |
|
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candidiasis, familial, type 4
|
MONDO:0013140 |
|