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Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
MMP2
(HGNC:7166)
multicentric osteolysis-nodulosis-arthropathy spectrum
(MONDO_0018298)
 Definitive
MMP14
(HGNC:7160)
multicentric osteolysis-nodulosis-arthropathy spectrum
(MONDO_0018298)
 Moderate
MMP14
(HGNC:7160)
Winchester syndrome
(MONDO_0010201)
 Moderate
MMP13
(HGNC:7159)
metaphyseal anadysplasia
(MONDO_0015177)
 Moderate
MMP13
(HGNC:7159)
metaphyseal chondrodysplasia, Spahr type
(MONDO_0009597)
 Strong
MLYCD
(HGNC:7150)
malonic aciduria
(MONDO_0009556)
 Definitive
TRPM1
(HGNC:7146)
congenital stationary night blindness
(MONDO_0016293)
 Definitive
ARSA
(HGNC:713)
metachromatic leukodystrophy
(MONDO_0018868)
 Definitive
ARSA
(HGNC:713)
metachromatic leukodystrophy, juvenile form
(MONDO_0009591)
 Definitive
KMT2D
(HGNC:7133)
Kabuki syndrome
(MONDO_0016512)
 Definitive
KMT2A
(HGNC:7132)
Wiedemann-Steiner syndrome
(MONDO_0011518)
 Definitive
MLH1
(HGNC:7127)
hereditary breast carcinoma
(MONDO_0016419)
 Limited
MLH1
(HGNC:7127)
Lynch syndrome 2
(MONDO_0012249)
 Definitive
MLH1
(HGNC:7127)
mismatch repair cancer syndrome 1
(MONDO_0010159)
 Definitive
MLH1
(HGNC:7127)
prostate cancer
(MONDO_0008315)
 Moderate
MLH1
(HGNC:7127)
ovarian cancer
(MONDO_0008170)
 Strong
MLH1
(HGNC:7127)
breast cancer
(MONDO_0007254)
 Limited
MLH1
(HGNC:7127)
Muir-Torre syndrome
(MONDO_0008018)
 Strong
MLH1
(HGNC:7127)
Lynch syndrome
(MONDO_0005835)
 Definitive
MLH1
(HGNC:7127)
rhabdomyosarcoma
(MONDO_0005212)
 Limited
Showing 821–840 of 6681