Bannayan-Riley-Ruvalcaba syndrome
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(Orphanet:109)
|
Cronkhite-Canada syndrome
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(Orphanet:2930)
|
ENTEROCOLITIS
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(OMIM:226150)
|
Generalized juvenile polyposis/juvenile polyposis coli
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(Orphanet:329971)
|
HERMANSKY-PUDLAK SYNDROME 1
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(OMIM:203300)
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Hereditary hemorrhagic telangiectasia
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(Orphanet:774)
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Hermansky-Pudlak syndrome with pulmonary fibrosis
|
(Orphanet:231500)
|
INFLAMMATORY BOWEL DISEASE 11
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(OMIM:191390)
|
INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE
|
(OMIM:613148)
|
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME
|
(OMIM:175050)
|
Juvenile polyposis syndrome
|
(Orphanet:2929)
|
Multiple intestinal atresia
|
(Orphanet:2300)
|
Neonatal inflammatory skin and bowel disease
|
(Orphanet:294023)
|
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications
|
(Orphanet:3018)
|
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER
|
(OMIM:187300)
|
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2
|
(OMIM:600376)
|
WISKOTT-ALDRICH SYNDROME
|
(OMIM:277970)
|
Wiskott-Aldrich syndrome
|
(Orphanet:906)
|