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:
ABC transporter disorders
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v
t
e
Genetic disorder
, membrane:
ABC transporter
disorders
ABCA
ABCA1
(
Tangier disease
)
ABCA3
(
Surfactant metabolism dysfunction 3
)
ABCA4
(
Stargardt disease 1
,
Retinitis pigmentosa 19
)
ABCA12
(
Harlequin-type ichthyosis
,
Lamellar ichthyosis 2
)
ABCB
ABCB4
(
Progressive familial intrahepatic cholestasis 3
)
ABCB7
(
ASAT
)
ABCB11
(
Progressive familial intrahepatic cholestasis 2
)
ABCC
ABCC2
(
Dubin–Johnson syndrome
)
ABCC6
(
Pseudoxanthoma elasticum
)
ABCC7
(
Cystic fibrosis
)
ABCC8
(
HHF1
,
TNDM2
)
ABCC9
(
Dilated cardiomyopathy 1O
)
ABCD
ABCD1
(
Adrenoleukodystrophy
,
Adrenomyeloneuropathy
)
ABCG
ABCG5
(
Sitosterolemia
)
ABCG8
(
Gallbladder disease
4,
Sitosterolemia
)
see also
ABC transporters
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:
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