Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
NDUFA3
(HGNC:7686)
Leigh syndrome
(MONDO_0009723)
 Moderate
NDST1
(HGNC:7680)
autosomal recessive non-syndromic intellectual disability
(MONDO_0019502)
 Moderate
NDUFA2
(HGNC:7685)
Leigh syndrome
(MONDO_0009723)
 Limited
NDUFA1
(HGNC:7683)
mitochondrial complex I deficiency
(MONDO_0100133)
 Moderate
NDUFA1
(HGNC:7683)
Leigh syndrome
(MONDO_0009723)
 Limited
MYL3
(HGNC:7584)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Limited
NDRG1
(HGNC:7679)
Charcot-Marie-Tooth disease type 4D
(MONDO_0011085)
 Strong
NCF4
(HGNC:7662)
chronic granulomatous disease
(MONDO_0018305)
 Strong
NCF2
(HGNC:7661)
chronic granulomatous disease
(MONDO_0018305)
 Definitive
MYL3
(HGNC:7584)
hypertrophic cardiomyopathy
(MONDO_0005045)
 Definitive
NBN
(HGNC:7652)
hereditary breast carcinoma
(MONDO_0016419)
 Limited
NBN
(HGNC:7652)
Nijmegen breakage syndrome
(MONDO_0009623)
 Definitive
MYL3
(HGNC:7584)
dilated cardiomyopathy
(MONDO_0005021)
 Moderate
NAGA
(HGNC:7631)
alpha-N-acetylgalactosaminidase deficiency
(MONDO_0017779)
 Limited
NBN
(HGNC:7652)
prostate cancer
(MONDO_0008315)
 Moderate
NAGA
(HGNC:7631)
alpha-N-acetylgalactosaminidase deficiency type 1
(MONDO_0012221)
 Strong
MYOC
(HGNC:7610)
congenital glaucoma
(MONDO_0020366)
 Limited
MYT1
(HGNC:7622)
craniofacial microsomia
(MONDO_0015397)
 Moderate
MYL2
(HGNC:7583)
congenital fiber-type disproportion myopathy
(MONDO_0009711)
 Limited
MYL2
(HGNC:7583)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Limited
Showing 681–700 of 6699