Disease
|
LncRNAs
|
abdominal aortic aneurysm
|
CDKN2B-AS1
|
acute kidney injury
|
MGAT3-AS1
|
acute lymphoblastic leukemia
|
CDKN2B-AS1, LOH12CR2
|
adolescent idiopathic scoliosis
|
CCDC18-AS1
|
affective disorders
|
DISC2
|
AIDS
|
NRON, 7SK, 7SL
|
alcoholic liver disease
|
AIRN
|
alveolar capillary dysplasia with misalignment of pulmonary veins
|
LINC01081, LINC01082
|
Alzheimer's disease
|
SNHG3, LINC01616, LINC01080, BACE1-AS, BCYRN1, HAR1A, SOX2-OT
|
amnestic mild cognitive impairment
|
LINC01080
|
anorexia nervosa
|
LINC00235
|
autism spectrum disorder
|
DISC2, LINC00942, FOXG1-AS1
|
autoimmune disease
|
GAS5
|
autoimmune thyroid disease
|
ZFAT-AS1
|
Beckwith-Wiedemann syndrome
|
KCNQ1OT1
|
bipolar disorder
|
DISC2, DAOA-AS1
|
blepharophimosis syndrome
|
BPESC1, PISRT1
|
bone diseases
|
DANCR
|
cardiac hypertrophy
|
7SK
|
cardiometabolic disease
|
ABHD15-AS1, CDKN2B-AS1, MIR222HG, NPSR1-AS1
|
cat eye syndrome
|
CECR3, CECR5-AS1, CECR7, CECR9
|
chronic lymphocytic leukemia
|
DLEU1, MIR155HG
|
chronic myeloid leukemia
|
MEG3
|
chronic nonalcoholic liver disease
|
AIRN
|
congenital hyperinsulinism
|
H19
|
coronary heart disease
|
CDKN2B-AS1
|
depression
|
DISC2, PWAR4
|
dermatomyositis
|
7SL
|
diabetes
|
CDKN2B-AS1, MALAT1, MEG3, LINC00673, LINC01512, LINC01574, TUNAR, IGF2-AS, PVT1
|
DiGeorge syndrome
|
DGCR11, DGCR12, DGCR10, DGCR5, DGCR9
|
Duchenne muscular dystrophy
|
LINCMD1
|
endometriosis
|
CDKN2B-AS1
|
facioscapulohumeral muscular dystrophy
|
DBET
|
growth restriction
|
H19
|
heart failure
|
FENDRR, MT-LIPCAR
|
heart pathological hypertrophy
|
MHRT
|
spinocerebellar ataxia type 8
|
ATXN8OS
|
Huntington's disease
|
HAR1A, TUG1, MEG3, NOP14-AS1, HTT-AS, BDNF-AS, HAR1B
|
infertility
|
H19, NEAT1
|
influenza A virus (IAV) infection
|
NRAV
|
intervertebral disc degeneration
|
LINC00917, LINC01562
|
intracranial aneurism
|
CDKN2B-AS1
|
ischemic stroke
|
CDKN2B-AS1
|
kawasaki disease
|
THRIL
|
keloid
|
CACNA1G-AS1
|
keratolytic winter erythema
|
LINC00529
|
Klinefelter's syndrome
|
XIST
|
leukemia
|
BGLT3, TCL, LAMP5-AS1
|
liver cirrhosis
|
APTR
|
lymphocytic leukemia
|
DLEU2
|
macrosomia
|
LINC00237
|
macrocephaly
|
LINC00237
|
malaria
|
MIF-AS1
|
Marek's disease
|
H19
|
Mullerian aplasia
|
H19
|
multiple sclerosis
|
IFNG-AS1
|
myelodysplastic syndrome
|
MEG3, SNHG4
|
myeloid leukemia
|
MIR99AHG, MIR100HG
|
myeloproliferative polycythaemia vera
|
H19
|
myocardial infarction
|
CDKN2B-AS1, MIAT
|
narcolepsy
|
LINC00165
|
neural tube defects
|
H19
|
neurodevelopmental syndromes
|
SOX2-OT
|
obesity
|
H19, BDNF-AS, SNHG11, LINC00237
|
pancreaticobiliary maljunction
|
UCA1
|
periodontitis
|
CDKN2B-AS1
|
Prader-Willi syndrome
|
MKRN3-AS1, SNHG14, PWRN1, PWRN2, IPW, PWARSN, MKRN3-AS1, H19, MEG8
|
pre-eclampsia
|
H19
|
preterm birth
|
LIFR-AS1
|
primary spontaneous pneumothorax
|
LINC00977
|
pseudohypoparathyroidism type Ib
|
GNAS-AS1
|
psoriasis
|
PTCSC3, PRINS,LINC01185
|
psychiatric disease
|
BDNF-AS
|
rheumatoid arthritis
|
HOTAIR
|
schizophrenia
|
DISC2, HAR1A, DAOA-AS1, BDNF-AS, HAR1B, DLG2-AS1, MIR137HG
|
scleroderma
|
TSIX
|
Sézary syndrome
|
DNM3OS
|
Silver-Russell syndrome
|
H19, MESTIT1
|
skeletal myogenesis
|
YAM1
|
Smith-Magenis syndrome
|
SMCR6
|
spinocerebellar ataxia
|
SCAANT1, ATXN8OS
|
syndromic developmental defect
|
MIR17HG
|
systemic lupus erythaematosus
|
GAS5, LINC01420
|
Usher syndrome type 3
|
CLRN1-AS1
|
ventricular septal defects
|
SMAD1-AS1
|
West Syndrome
|
LINC00581
|
Wiedemann-Beckwith syndrome
|
H19
|