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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
INTS13
(HGNC:20174)
|
intellectual disability
(MONDO_0001071)
|
Limited
|
|
|
ASPG
(HGNC:20123)
|
aspartylglucosaminuria
(MONDO_0008830)
|
Strong
|
|
|
ABHD4
(HGNC:20154)
|
anorexia nervosa
(MONDO_0005351)
|
Limited
|
|
|
TEDC1
(HGNC:20127)
|
autosomal recessive primary microcephaly
(MONDO_0016660)
|
Limited
|
|
|
FLVCR2
(HGNC:20105)
|
Fowler syndrome
(MONDO_0009168)
|
Definitive
|
|
|
CHURC1
(HGNC:20099)
|
autism
(MONDO_0005260)
|
Limited
|
|
|
ZNF408
(HGNC:20041)
|
exudative vitreoretinopathy
(MONDO_0019516)
|
Moderate
|
|
|
USP46
(HGNC:20075)
|
essential tremor
(MONDO_0003233)
|
Limited
|
|
|
USP36
(HGNC:20062)
|
premature menopause
(MONDO_0001119)
|
Limited
|
|
|
ADAM20
(HGNC:199)
|
Alzheimer disease
(MONDO_0004975)
|
Limited
|
|
|
PLSCR5
(HGNC:19952)
|
bipolar disorder
(MONDO_0004985)
|
Limited
|
|
|
MYORG
(HGNC:19918)
|
basal ganglia calcification, idiopathic, 1
(MONDO_0024538)
|
Strong
|
|
|
SCARF2
(HGNC:19869)
|
van den Ende-Gupta syndrome
(MONDO_0010959)
|
Strong
|
|
|
MMRN2
(HGNC:19888)
|
Parkinson disease
(MONDO_0005180)
|
Limited
|
|
|
GBP5
(HGNC:19895)
|
ovarian cancer
(MONDO_0008170)
|
Limited
|
|
|
POU2F3
(HGNC:19864)
|
psoriasis
(MONDO_0005083)
|
Limited
|
|
|
TC2N
(HGNC:19859)
|
von Willebrand disease (hereditary or acquired)
(MONDO_0024574)
|
Disputed
|
|
|
EPB41L4B
(HGNC:19818)
|
colorectal cancer
(MONDO_0005575)
|
Limited
|
|
|
UTP4
(HGNC:1983)
|
hereditary North American Indian childhood cirrhosis
(MONDO_0011497)
|
Moderate
|
|
|
TSSK4
(HGNC:19825)
|
male infertility
(MONDO_0005372)
|
Limited
|
|