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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
IFT52
(HGNC:15901)
|
ciliopathy
(MONDO_0005308)
|
Moderate
|
|
|
IFT52
(HGNC:15901)
|
cranioectodermal dysplasia
(MONDO_0009032)
|
Limited
|
|
|
CCNF
(HGNC:1591)
|
amyotrophic lateral sclerosis
(MONDO_0004976)
|
Moderate
|
|
|
TP53TG5
(HGNC:15856)
|
intellectual disability
(MONDO_0001071)
|
Limited
|
|
|
GZF1
(HGNC:15808)
|
Larsen syndrome
(MONDO_0007875)
|
Moderate
|
|
|
MOCS3
(HGNC:15765)
|
sulfite oxidase deficiency due to molybdenum cofactor deficiency
(MONDO_0020480)
|
Limited
|
|
|
MYL9
(HGNC:15754)
|
megacystis-microcolon-intestinal hypoperistalsis syndrome
(MONDO_0025986)
|
Moderate
|
|
|
BPIFA1
(HGNC:15749)
|
lung cancer
(MONDO_0008903)
|
Limited
|
|
|
BPIFA1
(HGNC:15749)
|
nasopharyngeal carcinoma
(MONDO_0015459)
|
Limited
|
|
|
MYL9
(HGNC:15754)
|
visceral myopathy 1
(MONDO_0020754)
|
Limited
|
|
|
KIRREL1
(HGNC:15734)
|
steroid-resistant nephrotic syndrome
(MONDO_0044765)
|
Limited
|
|
|
RASSF9
(HGNC:15739)
|
familial colorectal cancer type X
(MONDO_0018604)
|
Refuted
|
|
|
B3GNT2
(HGNC:15629)
|
muscular dystrophy-dystroglycanopathy, type A
(MONDO_0000171)
|
Limited
|
|
|
SLC12A8
(HGNC:15595)
|
psoriasis
(MONDO_0005083)
|
Limited
|
|
|
SYTL2
(HGNC:15585)
|
colorectal cancer
(MONDO_0005575)
|
Limited
|
|
|
CBX7
(HGNC:1557)
|
plasma cell myeloma
(MONDO_0009693)
|
Limited
|
|
|
EPPK1
(HGNC:15577)
|
childhood acute lymphoblastic leukemia
(MONDO_0000870)
|
Limited
|
|
|
CBX4
(HGNC:1554)
|
hepatocellular carcinoma
(MONDO_0007256)
|
Limited
|
|
|
CBX2
(HGNC:1552)
|
schizophrenia
(MONDO_0005090)
|
Limited
|
|
|
FAM167A
(HGNC:15549)
|
systemic lupus erythematosus
(MONDO_0007915)
|
Moderate
|
|