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
HOXB6
(HGNC:5117)
hypospadias
(MONDO_0005345)
 Limited
HOXB4
(HGNC:5115)
acute myeloid leukemia
(MONDO_0018874)
 Limited
HOXA7
(HGNC:5108)
acute myeloid leukemia
(MONDO_0018874)
 Limited
HOXA4
(HGNC:5105)
hypospadias
(MONDO_0005345)
 Limited
HNRNPK
(HGNC:5044)
Au-Kline syndrome
(MONDO_0014700)
 Strong
HOXA4
(HGNC:5105)
lung adenocarcinoma
(MONDO_0005061)
 Limited
HNRNPH3
(HGNC:5043)
salivary duct carcinoma
(MONDO_0044915)
 Limited
RIPK4
(HGNC:496)
Bartsocas-Papas syndrome 1
(MONDO_0009901)
 Strong
HLX
(HGNC:4978)
congenital diaphragmatic hernia
(MONDO_0005711)
 Limited
HK3
(HGNC:4925)
premature menopause
(MONDO_0001119)
 Limited
ANGPTL2
(HGNC:490)
Schimke immuno-osseous dysplasia
(MONDO_0009458)
 Refuted
HCCS
(HGNC:4837)
linear skin defects with multiple congenital anomalies 1
(MONDO_0024552)
 Strong
HARS2
(HGNC:4817)
Perrault syndrome
(MONDO_0017312)
 Strong
H2BC15 Gene
(HGNC:4749)
prostate cancer
(MONDO_0008315)
 Limited
GYG2
(HGNC:4700)
Leigh syndrome
(MONDO_0009723)
 Limited
GTPBP2
(HGNC:4670)
Jaberi-Elahi syndrome
(MONDO_0060711)
 Moderate
GYG2
(HGNC:4700)
glycogen storage disease II
(MONDO_0009290)
 Disputed
GUCY1B1
(HGNC:4687)
hypertensive disorder
(MONDO_0005044)
 Moderate
GTF3C5
(HGNC:4668)
type 1 diabetes mellitus
(MONDO_0005147)
 Limited
GTF2E2
(HGNC:4651)
trichothiodystrophy
(MONDO_0018053)
 Moderate
Showing 5421–5440 of 6699