Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
SDHB
(HGNC:10681)
mitochondrial disease
(MONDO_0044970)
 Moderate
SDHB
(HGNC:10681)
Cowden disease
(MONDO_0016063)
 Limited
SDHB
(HGNC:10681)
Carney-Stratakis syndrome
(MONDO_0011740)
 Moderate
SDHB
(HGNC:10681)
gastrointestinal stromal tumor
(MONDO_0011719)
 Strong
SDHB
(HGNC:10681)
renal cell carcinoma
(MONDO_0005086)
 Moderate
SDHB
(HGNC:10681)
pheochromocytoma
(MONDO_0008233)
 Definitive
SDHA
(HGNC:10680)
mitochondrial complex II deficiency, nuclear type 1
(MONDO_0100294)
 Strong
SDHA
(HGNC:10680)
gastrointestinal stromal tumor
(MONDO_0011719)
 Strong
SDCCAG8
(HGNC:10671)
Senior-Loken syndrome
(MONDO_0017842)
 Limited
SDCCAG8
(HGNC:10671)
Bardet-Biedl syndrome
(MONDO_0015229)
 Strong
SDHA
(HGNC:10680)
Leigh syndrome
(MONDO_0009723)
 Moderate
TSHZ1
(HGNC:10669)
aural atresia, congenital
(MONDO_0011921)
 Moderate
TSHZ1
(HGNC:10669)
congenital vertical talus
(MONDO_0008652)
 Limited
SCO1
(HGNC:10603)
mitochondrial disease
(MONDO_0044970)
 Moderate
AIMP1
(HGNC:10648)
hypomyelinating leukodystrophy 3
(MONDO_0009843)
 Moderate
SCP2
(HGNC:10606)
sterol carrier protein 2 deficiency
(MONDO_0013391)
 Moderate
SCO2
(HGNC:10604)
Leigh syndrome
(MONDO_0009723)
 Moderate
SCNN1B
(HGNC:10600)
pseudohypoaldosteronism, type IB1, autosomal recessive
(MONDO_0009917)
 Limited
SCNN1A
(HGNC:10599)
pseudohypoaldosteronism, type IB1, autosomal recessive
(MONDO_0009917)
 Strong
SCNN1G
(HGNC:10602)
pseudohypoaldosteronism, type IB1, autosomal recessive
(MONDO_0009917)
 Moderate
Showing 4221–4240 of 6699