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Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries
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Gene Disease Score Actions
LMX1B
(HGNC:6654)
nail-patella-like renal disease
(MONDO_0009724)
 Strong
LMX1B
(HGNC:6654)
nail-patella syndrome
(MONDO_0008061)
 Definitive
LMNB1
(HGNC:6637)
adult-onset autosomal dominant demyelinating leukodystrophy
(MONDO_0008215)
 Definitive
LMX1A
(HGNC:6653)
Mobius syndrome
(MONDO_0008006)
 Limited
LMOD3
(HGNC:6649)
nemaline myopathy 10
(MONDO_0014513)
 Strong
LMNA
(HGNC:6636)
Emery-Dreifuss muscular dystrophy 2, autosomal dominant
(MONDO_0021569)
 Definitive
LMNA
(HGNC:6636)
atypical Werner syndrome
(MONDO_0019321)
 Strong
LMNA
(HGNC:6636)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Moderate
LMNA
(HGNC:6636)
congenital muscular dystrophy due to LMNA mutation
(MONDO_0013178)
 Strong
LMNA
(HGNC:6636)
mandibuloacral dysplasia with type A lipodystrophy
(MONDO_0009557)
 Moderate
LMNA
(HGNC:6636)
Charcot-Marie-Tooth disease type 2B1
(MONDO_0011569)
 Strong
LMNA
(HGNC:6636)
Hutchinson-Gilford progeria syndrome
(MONDO_0008310)
 Definitive
LMNA
(HGNC:6636)
familial partial lipodystrophy, Dunnigan type
(MONDO_0007906)
 Strong
LMNA
(HGNC:6636)
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
(MONDO_0008915)
 Disputed
LMNA
(HGNC:6636)
dilated cardiomyopathy 1A
(MONDO_0007269)
 Strong
LMNA
(HGNC:6636)
dilated cardiomyopathy
(MONDO_0005021)
 Definitive
LMNA
(HGNC:6636)
atrial fibrillation
(MONDO_0004981)
 Limited
LMNA
(HGNC:6636)
atrioventricular block
(MONDO_0000465)
 Strong
LMAN1
(HGNC:6631)
combined deficiency of factor V and factor VIII
(MONDO_0018175)
 Definitive
LIPE
(HGNC:6621)
LIPE-related familial partial lipodystrophy
(MONDO_0014431)
 Moderate
Showing 961–980 of 6681