released

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

MONDO:0010459

amyotrophic lateral sclerosis type 15

ffac462a-1554-402c-9018-5e906e0f4cff

released

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

MONDO:0007453

maturity-onset diabetes of the young type 2

e1f26c43-eeb7-439d-9f69-c771e291b8e0

released

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

MONDO:0005147

type 1 diabetes mellitus

bf706762-9df7-4eba-9d18-b56848001059

released

MEDS1, primary microcephaly-epilepsy-permanent neonatal diabetes syndrome

MONDO:0031481

microcephaly, epilepsy, and diabetes syndrome 1

bf1abaf4-f95c-4642-b68f-2268106b89f5

released

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

MONDO:0011236

hyperinsulinism due to glucokinase deficiency

a6cef23d-7f25-4d41-a710-ad6f24f7e4d5

released

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

MONDO:0005406

gestational diabetes

a493647d-23e9-4174-8cc7-00a069a800bd

released

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

MONDO:0016391

neonatal diabetes mellitus

8ed2205e-b7e5-4ab1-bd6c-5744f77845c4

released

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

MONDO:0005015

diabetes mellitus

839771db-7adf-4373-93cd-450588fb32a3

released

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

MONDO:0005148

type 2 diabetes mellitus

78a0e522-1e1f-4193-88c0-42af38a29093

released

monogenic diabetes, rare genetic diabetes mellitus

MONDO:0015967

monogenic diabetes

7486f60c-707a-4d19-8b9f-6efcd0b9957d

released

diabetes mellitus, permanent neonatal 1, PNDM1

MONDO:0100165

permanent neonatal diabetes mellitus 1

55868b84-eaa6-432c-bc7e-fa18ffa3dfa1

released

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

MONDO:0100164

permanent neonatal diabetes mellitus

504a8e1c-8c5d-446e-9766-5ad84ab30d8d

released

MONDO:0009416

hypoinsulinemic hypoglycemia and body hemihypertrophy

4db73329-ea25-4275-acf9-2d747cbae071

released

MONDO:0100328

microcephaly, epilepsy, and diabetes syndrome

124c8e42-c68b-48bd-b209-1739e613df74

released

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

MONDO:0017182

familial hyperinsulinism

0bb28c64-c93e-4106-a790-36427fdbea6d

released

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

MONDO:0011582

multiple mitochondrial dysfunctions syndrome 1

030c980c-2b90-4c08-912d-efb73262c4f9