Stats
Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
CHRNE
(HGNC:1966)
|
congenital myasthenic syndrome 4C
(MONDO_0012157)
|
Strong
|
|
|
CHRNG
(HGNC:1967)
|
lethal multiple pterygium syndrome
(MONDO_0009668)
|
Moderate
|
|
|
CHRNB2
(HGNC:1962)
|
sleep-related hypermotor epilepsy
(MONDO_0000030)
|
Moderate
|
|
|
SCAF4
(HGNC:19304)
|
Fliedner-Zweier syndrome
(MONDO_0957787)
|
Moderate
|
|
|
CHRNA7
(HGNC:1960)
|
complex neurodevelopmental disorder
(MONDO_0100038)
|
Limited
|
|
|
CHRNB4
(HGNC:1964)
|
lung cancer
(MONDO_0008903)
|
Limited
|
|
|
CHRNA7
(HGNC:1960)
|
epilepsy
(MONDO_0005027)
|
Limited
|
|
|
CHRNA4
(HGNC:1958)
|
autosomal dominant nocturnal frontal lobe epilepsy
(MONDO_0020300)
|
Strong
|
|
|
ADAM17
(HGNC:195)
|
inflammatory skin and bowel disease, neonatal, 1
(MONDO_0013693)
|
Strong
|
|
|
HYDIN
(HGNC:19368)
|
primary ciliary dyskinesia
(MONDO_0016575)
|
Strong
|
|
|
ADAM17
(HGNC:195)
|
congenital heart disease
(MONDO_0005453)
|
Limited
|
|
|
CHRNA2
(HGNC:1956)
|
autosomal dominant nocturnal frontal lobe epilepsy
(MONDO_0020300)
|
Moderate
|
|
|
CHRNA4
(HGNC:1958)
|
sleep-related hypermotor epilepsy
(MONDO_0000030)
|
Strong
|
|
|
CHRNA2
(HGNC:1956)
|
benign familial infantile epilepsy
(MONDO_0017615)
|
Limited
|
|
|
CHRNA1
(HGNC:1955)
|
lethal multiple pterygium syndrome
(MONDO_0009668)
|
Moderate
|
|
|
ADA
(HGNC:186)
|
Omenn syndrome
(MONDO_0011338)
|
Limited
|
|
|
SBDS
(HGNC:19440)
|
Shwachman-Diamond syndrome
(MONDO_0009833)
|
Definitive
|
|
|
CHRNA1
(HGNC:1955)
|
postsynaptic congenital myasthenic syndrome
(MONDO_0020344)
|
Moderate
|
|
|
ZMYND10
(HGNC:19412)
|
primary ciliary dyskinesia
(MONDO_0016575)
|
Strong
|
|
|
SOCS4
(HGNC:19392)
|
autoimmune disease
(MONDO_0007179)
|
Limited
|
|