All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
07170 CAKUT Congenital Anomalies of the Kidney and Urinary Tract accompanied by cryptorchidism 603054 AD - - GREM1 kidney Renal hypoplasia, dysplasia, hydronephrosis (ureteropelvic junction obstruction or ureterovesical junction obstruction), ureteric duplex, vesicoureteral reflux, and posterior urethral valves. Possibly with cryptorchidism.
07169 HMPS Hereditary Mixed Polyposis Syndrome 601228 AD 2 2 GREM1 rectum Large intestinal polyposis, in which both a mixture of polyps of different histological types are seen, and there may be polyps which have mixed histology, i.e. more than one type in the same polyp. The condition predisposes to adenocarcinoma of the colon and rectum. See PMID 9024286; 14572586; 18807306; 27984123;
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