|
TYROBP
(HGNC:12449)
|
polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly
(MONDO_0009092)
|
Definitive
|
|
|
TYR
(HGNC:12442)
|
oculocutaneous albinism type 1
(MONDO_0018135)
|
Definitive
|
|
|
TTR
(HGNC:12405)
|
amyloidosis, hereditary systemic 1
(MONDO_0971004)
|
Definitive
|
|
|
TYR
(HGNC:12442)
|
oculocutaneous albinism type 1B
(MONDO_0011749)
|
Strong
|
|
|
TTN
(HGNC:12403)
|
autosomal recessive limb-girdle muscular dystrophy type 2J
(MONDO_0012127)
|
Moderate
|
|
|
TTR
(HGNC:12405)
|
familial amyloid neuropathy
(MONDO_0007100)
|
Definitive
|
|
|
TTN
(HGNC:12403)
|
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
|
Limited
|
|
|
TYR
(HGNC:12442)
|
oculocutaneous albinism type 1A
(MONDO_0008745)
|
Definitive
|
|
|
TTN
(HGNC:12403)
|
myopathy, myofibrillar, 9, with early respiratory failure
(MONDO_0011362)
|
Strong
|
|
|
TYK2
(HGNC:12440)
|
immunodeficiency 35
(MONDO_0012682)
|
Strong
|
|
|
C1QB
(HGNC:1242)
|
C1Q deficiency
(MONDO_0013343)
|
Strong
|
|
|
TTN
(HGNC:12403)
|
congenital myopathy
(MONDO_0019952)
|
Strong
|
|
|
C1QBP
(HGNC:1243)
|
mitochondrial disease
(MONDO_0044970)
|
Limited
|
|
|
C1QBP
(HGNC:1243)
|
combined oxidative phosphorylation deficiency 33
(MONDO_0054677)
|
Limited
|
|
|
TULP3
(HGNC:12425)
|
hepatorenocardiac degenerative fibrosis
(MONDO_0859254)
|
Limited
|
|
|
TWIST1
(HGNC:12428)
|
Sweeney-Cox syndrome
(MONDO_0060592)
|
Moderate
|
|
|
TULP3
(HGNC:12425)
|
ciliopathy
(MONDO_0005308)
|
Strong
|
|
|
TTN
(HGNC:12403)
|
early-onset myopathy with fatal cardiomyopathy
(MONDO_0012714)
|
Moderate
|
|
|
TTN
(HGNC:12403)
|
hypertrophic cardiomyopathy
(MONDO_0005045)
|
Disputed
|
|
|
TTN
(HGNC:12403)
|
dilated cardiomyopathy
(MONDO_0005021)
|
Definitive
|
|