All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03200 EIG-8 epilepsy, idiopathic, generalized, susceptibility to, type 8 (EIG-8) 612899 6 6 CASR - -
00890 HHC-1 Hypocalciuric hypercalcemia, type I (HHC-1) 145980 169 167 CASR - -
02345 HYPOC-1 hypocalcemia, autosomal dominant, Bartter syndrome incl. (HYPOC-1) 601198 105 88 CASR - autosomal dominant
00891 NSHPT hyperparathyroidism, severe, neonatal (NSHPT) 239200 45 28 CASR - autosomal dominant/autosomal recessive