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Details on Person vitamin metabolic disorder

Class:IdDisease:3325582
_displayNamevitamin metabolic disorder
_timestamp2013-05-10 12:28:47
created[InstanceEdit:3325583] Jassal, B, 2013-05-10
definitionAn inherited metabolic disorder resulting from a deficiency in vitamin or vitamin cofactor transport or metabolism.
identifier0050718
namevitamin metabolic disorder
referenceDatabase[ReferenceDatabase:1247631] DOID
(disease)[EntityWithAccessionedSequence:3325442] HLCS R508W [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:3325460] HLCS V550M [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:3325463] HLCS G261Vfs*20 [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:3325499] HLCS D571N [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:3325506] HLCS G581S [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:3325513] HLCS L216R [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:3325514] HLCS L237P [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:3325543] BTD R538C [extracellular region] [Homo sapiens]
[EntityWithAccessionedSequence:3325545] BTD R79C [extracellular region] [Homo sapiens]
[EntityWithAccessionedSequence:3325552] BTD Q456H [extracellular region] [Homo sapiens]
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No pathways have been reviewed or authored by vitamin metabolic disorder (3325582)