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

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

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

primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MEDS1

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

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

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

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

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

monogenic diabetes, rare genetic diabetes mellitus

diffuse systemic sclerosis, systemic sclerosis, diffuse

diabetes mellitus, permanent neonatal 1, PNDM1

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

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

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