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Gene–disease association summaries
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
|
|