All diseases

17 entries on 1 page. Showing entries 1 - 17.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01730 - cryptorchidism 219050 AD - - INSL3, RXFP2 - -
02015 - Rabson-Mendenhall syndrome 262190 AR 2 2 INSR - -
02957 - Insulin-resistant diabetes mellitus and acanthosis nigricans 610549 - 3 3 INSR - -
02888 HHF5 Hyperinsulinemic hypoglycemia familial 5 609968 AD - - INSR - -
04520 hyperproinsulinemia hyperproinsulinemia 616214 AD - - INS - -
00150 IDDM diabetes mellitus, insulin-dependent (IDDM) 222100 AR 8 8 FOXP3, HNF1A, IL6, INS, ITPR3, OAS1, PTPN22 - -
01287 IDDM2 diabetes mellitus, insulin-dependent, type 2 (IDDM2) 125852 AD 2 2 INS - -
06514 IMD55 Immunodeficiency 55 617827 AR - - GINS1 - -
01893 LEPRECHAUNISM Leprechaunism (Donohue syndrome) 246200 AR - - INSR - -
05593 MODY diabetes of the young, maturity-onset (MODY) - - 3709 3706 INS, NEUROD1 - -
03317 MODY10 diabetes of the young, maturity-onset, type 10 (MODY10) 613370 AD 3 3 INS - -
04147 MRT mental retardation, autosomal recessive (MRT, intellectual disability (IDT)) - - 24 24 ELP2, LINGO1, LINS, MBOAT7, METTL5, PGAP1 - autosomal recessive
03611 MRT27 mental retardation, autosomal recessive, type 27 (MRT-27) 614340 AR 2 - LINS - -
05900 PNDM4 diabetes mellitus, permanent neonatal, type 4 (PNDM4) 618858 AD;AR - - INS - -
05148 SINO SINO syndrome (spastic paraplegia, intellectual disability, nystagmus, and obesity) - - 3 3 KIDINS220 - -
06465 SINO Spastic paraplegia, intellectual disability, nystagmus, and obesity 617296 AD - - KIDINS220 - -
04184 stature, short stature, short - - 89 78 GINS3 - -
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