|
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
|
|