ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY
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(OMIM:174770)
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AGAMMAGLOBULINEMIA, X-LINKED
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(OMIM:300755)
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IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTIONAND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST
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(OMIM:146840)
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INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE
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(OMIM:613148)
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Pyogenic arthritis - pyoderma gangrenosum - acne
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(Orphanet:69126)
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Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
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(Orphanet:632)
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Thymic aplasia
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(Orphanet:83471)
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