Autosomal recessive early-onset inflammatory bowel disease
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(Orphanet:238569)
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Cyclic neutropenia
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(Orphanet:2686)
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Familial caudal dysgenesis
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(Orphanet:1768)
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GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE
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(OMIM:233690)
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GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I
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(OMIM:233700)
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GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II
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(OMIM:233710)
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GRANULOMATOUS DISEASE, CHRONIC, X-LINKED
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(OMIM:306400)
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Leukocyte adhesion deficiency
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(Orphanet:2968)
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Leukocyte adhesion deficiency type I
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(Orphanet:99842)
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Neutropenia, severe congenital, 1, autosomal dominant
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(OMIM:202700)
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