amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant, amyotrophic lateral sclerosis 15, UBQLN2 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis caused by mutation in UBQLN2, amyotrophic lateral sclerosis type 15, ALS15

glucokinase-associated diabetes mellitus, GCK maturity-onset diabetes of the young (disease), maturity-onset diabetes of the young (disease) caused by mutation in GCK, MODY type 2, MODY glucokinase-related, GCK-associated diabetes mellitus, maturity onset diabetes of the Young, type 2, MODY, type II, MODY 2 monogenic diabetes type 2, MODY2

juvenile diabetes, type I diabetes mellitus, type 1 diabetes, IDDM, insulin-dependent diabetes mellitus, insulin dependent diabetes, diabetes mellitis type I, type I diabetes, diabetes mellitis type 1, immune mediated diabetes

MEDS1, primary microcephaly-epilepsy-permanent neonatal diabetes syndrome

hyperinsulinemic hypoglycemia due to glucokinase deficiency, hyperinsulinemic hypoglycemia, familial, type 3

gestational diabetes mellitus, GDM, maternal gestational diabetes mellitus, diabetes in pregnancy

diabetes mellitus syndrome in newborn infant, NDM, congenital diabetes mellitus

diabetes, diabetes mellitus (disease), DM, diabetes mellitus

non-insulin dependent diabetes, diabetes mellitus, type 2, diabetes mellitus, noninsulin-dependent, association with, adult onset diabetes, noninsulin-dependent diabetes mellitus, type 2 diabetes mellitus, insulin resistance, severe, digenic, non-insulin dependent diabetes mellitus, non-insulin-dependent diabetes mellitus, NIDDM, adult-onset diabetes, diabetes, type 2, diabetes mellitus, noninsulin-dependent, diabetes mellitis type 2, type 2 diabetes mellitus non-insulin dependent, noninsulin dependent diabetes, diabetes mellitis type II, diabetes mellitus, noninsulin-dependent, late onset, T2DM - type 2 diabetes mellitus, type II diabetes, type 2 diabetes, type II diabetes mellitus, diabetes mellitus, type II

monogenic diabetes, rare genetic diabetes mellitus

diabetes mellitus, permanent neonatal 1, PNDM1

PNDM, monogenic diabetes of infancy, PDMI, permanent diabetes mellitus of infancy

congenital hyperinsulinism, neonatal hyperinsulinism, hereditary hyperinsulinism (disease), FHI, HHI, nesidioblastosis, hyperinsulinemia of infancy, familial hyperinsulinemic hypoglycemia

NFU1 deficiency, multiple mitochondrial dysfunctions syndrome type 1, multiple mitochondrial dysfunctions syndrome 1, fatal multiple mitochondrial dysfunctions syndrome caused by mutation in NFU1, NFU1 fatal multiple mitochondrial dysfunctions syndrome