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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
SEMA4A
(HGNC:10729)
|
familial colorectal cancer type X
(MONDO_0018604)
|
Limited
|
|
|
SEMA4A
(HGNC:10729)
|
cone-rod dystrophy
(MONDO_0015993)
|
Limited
|
|
|
SELENBP1
(HGNC:10719)
|
schizophrenia
(MONDO_0005090)
|
Limited
|
|
|
SEC24D
(HGNC:10706)
|
Cole-Carpenter syndrome
(MONDO_0016085)
|
Moderate
|
|
|
SEC24D
(HGNC:10706)
|
Cole-Carpenter syndrome 2
(MONDO_0014573)
|
Moderate
|
|
|
SEC23B
(HGNC:10702)
|
congenital dyserythropoietic anemia
(MONDO_0019403)
|
Definitive
|
|
|
SEC23B
(HGNC:10702)
|
congenital dyserythropoietic anemia type 2
(MONDO_0009134)
|
Definitive
|
|
|
SDHC
(HGNC:10682)
|
gastrointestinal stromal tumor
(MONDO_0011719)
|
Strong
|
|
|
SEC23B
(HGNC:10702)
|
Cowden disease
(MONDO_0016063)
|
Limited
|
|
|
SDHD
(HGNC:10683)
|
Cowden disease
(MONDO_0016063)
|
Limited
|
|
|
BMP2
(HGNC:1069)
|
brachydactyly type A2
(MONDO_0007216)
|
Limited
|
|
|
SDHD
(HGNC:10683)
|
Carney-Stratakis syndrome
(MONDO_0011740)
|
Moderate
|
|
|
SDHD
(HGNC:10683)
|
mitochondrial disease
(MONDO_0044970)
|
Moderate
|
|
|
SDHD
(HGNC:10683)
|
pheochromocytoma
(MONDO_0008233)
|
Strong
|
|
|
SDHD
(HGNC:10683)
|
paragangliomas 1
(MONDO_0008192)
|
Strong
|
|
|
SDHC
(HGNC:10682)
|
mitochondrial disease
(MONDO_0044970)
|
Limited
|
|
|
SDHD
(HGNC:10683)
|
renal cell carcinoma
(MONDO_0005086)
|
Limited
|
|
|
SDHC
(HGNC:10682)
|
Carney-Stratakis syndrome
(MONDO_0011740)
|
Moderate
|
|
|
SDHC
(HGNC:10682)
|
Cowden disease
(MONDO_0016063)
|
Limited
|
|
|
SDHC
(HGNC:10682)
|
renal cell carcinoma
(MONDO_0005086)
|
Limited
|
|