SHMARQL

adult-onset autosomal recessive sideroblastic anemia

<http://www.wikidata.org/entity/Q56013627>

) described in a single patient with adult onset microcytic hypochromic anemia with liver iron overload and type 2 diabetes
rdfs:label
"adult-onset autosomal recessive sideroblastic anemia"@en
skos:altLabel "Anemia, Sideroblastic, 3, Pyridoxine-Refractory"@en
"GLRX5-related sideroblastic anemia"@en
"SIDBA3"@en
schema:description ") described in a single patient with adult onset microcytic hypochromic anemia with liver iron overload and type 2 diabetes"@en
schema:dateModified "2026-10-23T23:48:48+00:00"^^xsd:dateTime
schema:version 2560159125
wikibase:identifiers 8
wikibase:sitelinks 0
wikibase:statements 17
p:P1193 wd:statement/Q56013627-1B997B18-00A8-4E89-9181-C8058D2F949F
p:P14914 wd:statement/Q56013627-6B26ED87-93F1-4B91-9134-FA130A968C1E
p:P1550 wd:statement/Q56013627-00B87438-2437-4E41-9503-2AFE7F586D77
p:P2293 wd:statement/Q56013627-67826CF3-14A6-4316-A874-A8F9B1343A4A
wd:statement/Q56013627-88FCD0E9-0373-416D-87CE-7EE26E290434
p:P279 wd:statement/Q56013627-F4ABC2F5-D9C3-4908-98A2-A636F4C76E1F
p:P2841 wd:statement/Q56013627-7BCE6DAA-5B0A-43F2-B292-5276D6B6FCC0
p:P2888 wd:statement/Q56013627-CD743CB9-DCD1-40FB-A84D-2EB311A179C6
p:P2892 wd:statement/Q56013627-668FF220-26E5-43A1-ABBF-07A12B709DE5
wd:statement/Q56013627-BB090321-F719-4373-B67E-B2A70D2F4208
wd:statement/Q56013627-E9269E6A-2445-47F9-A9AF-A8C0D04E1EEA
p:P31 wd:statement/Q56013627-065ED0B1-6480-46CD-8A87-1BCC3373B7E7
wd:statement/Q56013627-BDE005C3-ABC5-4B12-917D-F85355809920
p:P4229 wd:statement/Q56013627-F9D6B15F-0CCA-4CF5-965D-897EF67C59A6
p:P492 wd:statement/Q56013627-CE3D3987-DCC0-49D9-9BDB-E9DE21BABF51
p:P5270 wd:statement/Q56013627-A237C1FF-9825-434C-B89F-623AE1B0C2D2
p:P6532 wd:statement/Q56013627-F95E496D-0071-4503-818E-26E9A19B05F2
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0014804>
wdt:P1193 0.000001^^xsd:decimal
wdt:P14914 "D255132"
wdt:P1550 "255132"
wdt:P2293 SLC25A38
GLRX5
wdt:P279 disease
wdt:P2841 adult onset
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_255132>
wdt:P2892 "C2673914"
"C4225155"
"C4304054"
wdt:P31 type of disease
rare disease
wdt:P4229 "D64.0"
wdt:P492 "616860"
wdt:P5270 "MONDO_0014804"
wdt:P6532 liver cirrhosis
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