Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
Back to Open Access Summaries

Gene–Disease Browser

Need updated, customized, evidence‑backed summaries? Get it from the leaders in AI‑powered, evidence‑backed summaries provider.
Contact us
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
Showing 4201–4220 of 6699