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
MT-CO3
(HGNC:7422)
Leber hereditary optic neuropathy
(MONDO_0010788)
 Limited
MT-CO3
(HGNC:7422)
Leigh syndrome
(MONDO_0009723)
 Limited
MT-CO2
(HGNC:7421)
mitochondrial disease
(MONDO_0044970)
 Moderate
MT-CO2
(HGNC:7421)
MELAS syndrome
(MONDO_0010789)
 Limited
MT-CO2
(HGNC:7421)
Leigh syndrome
(MONDO_0009723)
 Limited
MT-CO2
(HGNC:7421)
cytochrome-c oxidase deficiency disease
(MONDO_0009068)
 Moderate
MT-CO1
(HGNC:7419)
mitochondrial disease
(MONDO_0044970)
 Limited
MT-CO1
(HGNC:7419)
MELAS syndrome
(MONDO_0010789)
 Limited
MT-CO1
(HGNC:7419)
Leigh syndrome
(MONDO_0009723)
 Limited
MT-CO1
(HGNC:7419)
cytochrome-c oxidase deficiency disease
(MONDO_0009068)
 Limited
MT-ATP8
(HGNC:7415)
mitochondrial disease
(MONDO_0044970)
 Moderate
MT-ATP6
(HGNC:7414)
mitochondrial disease
(MONDO_0044970)
 Strong
MT-ATP6
(HGNC:7414)
NARP syndrome
(MONDO_0010794)
 Strong
MSH6
(HGNC:7329)
prostate cancer
(MONDO_0008315)
 Moderate
MT-ATP6
(HGNC:7414)
Leber hereditary optic neuropathy
(MONDO_0010788)
 Moderate
MT-ATP6
(HGNC:7414)
Leigh syndrome
(MONDO_0009723)
 Definitive
MSH6
(HGNC:7329)
ovarian cancer
(MONDO_0008170)
 Strong
MSX2
(HGNC:7392)
parietal foramina with cleidocranial dysplasia
(MONDO_0008198)
 Moderate
MSX1
(HGNC:7391)
tooth and nail syndrome
(MONDO_0008582)
 Moderate
MST1
(HGNC:7380)
epidermodysplasia verruciformis
(MONDO_0009176)
 Limited
Showing 781–800 of 6699