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Details on Person hypochromic microcytic anemia

Class:IdDisease:5623576
_displayNamehypochromic microcytic anemia
_timestamp2014-09-17 15:39:39
created[InstanceEdit:5623578] Jassal, Bijay, 2014-09-17
identifier0050642
namehypochromic microcytic anemia
referenceDatabase[ReferenceDatabase:1247631] DOID
(disease)[EntityWithAccessionedSequence:5623707] SLC11A2 L104_P142del [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:5623732] SLC11A2 E399D [plasma membrane] [Homo sapiens]
[DefinedSet:5623738] SLC11A2 mutants [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:5623747] SLC11A2 V114del [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:5623758] SLC11A2 R416C [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:5623771] SLC11A2 G212V [plasma membrane] [Homo sapiens]
[Pathway:5619048] Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1) [Homo sapiens]
[FailedReaction:5623558] Defective SLC11A2 does not cotransport Fe2+, H+ from extracellular region to cytosol [Homo sapiens]
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No pathways have been reviewed or authored by hypochromic microcytic anemia (5623576)