Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

6 matching diseasesClear search ×

OBSOLETE: Congenital sucrase-isomaltase deficiency without starch intolerance

OBSOLETE: CSID without starch intolerance · OBSOLETE: Disaccharide intolerance without starch intolerance

ORPHA:306462

Congenital sucrase-isomaltase deficiency

CSID · Congenital sucrose intolerance

ORPHA:35122

OBSOLETE: Congenital sucrase-isomaltase deficiency with minimal starch tolerance

OBSOLETE: CSID with minimal starch tolerance · OBSOLETE: Disaccharide intolerance with minimal starch tolerance

ORPHA:306446

OBSOLETE: Congenital sucrase-isomaltase deficiency with starch and lactose intolerance

OBSOLETE: Congenital sucrose intolerance with starch and lactose intolerance · OBSOLETE: Congenital sucrase-isomaltose malabsorption with starch and lactose intolerance

ORPHA:306474

OBSOLETE: Congenital sucrase-isomaltase deficiency with starch intolerance

OBSOLETE: CSID with starch intolerance · OBSOLETE: Disaccharide intolerance with starch intolerance

ORPHA:306436

OBSOLETE: Congenital sucrase-isomaltase deficiency without sucrose intolerance

OBSOLETE: CSID without sucrose intolerance · OBSOLETE: Disaccharide intolerance without sucrose intolerance

ORPHA:306486