Autosomal dominant hyper-IgE syndrome
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(Orphanet:2314)
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Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
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(Orphanet:331226)
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DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS
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(OMIM:221700)
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Desquamative interstitial pneumonia
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(Orphanet:98852)
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Epidermolytic palmoplantar keratoderma
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(Orphanet:2199)
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Generalized peeling skin syndrome
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(Orphanet:263543)
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IgE RESPONSIVENESS, ATOPIC
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(OMIM:147050)
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Lymphoid hypereosinophilic syndrome
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(Orphanet:314970)
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Netherton syndrome
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(Orphanet:634)
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Severe combined immunodeficiency due to adenosine deaminase deficiency
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(Orphanet:277)
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WISKOTT-ALDRICH SYNDROME
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(OMIM:301000)
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WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM
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(OMIM:600903)
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X-linked thrombocytopenia with normal platelets
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(Orphanet:852)
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