SHMARQL

sulfuraminoacidemia

<http://www.wikidata.org/entity/Q19001322>

Human disease
rdfs:label
"sulfuraminoacidemia"@en
skos:altLabel
"Cytosolic methyl group transfer or sulfur amino acid metabolism disorder"@en
"Disorder of methionine cycle and sulfur amino acid metabolism"@en
"Disturbance of sulfur-bearing amino acid metabolism NOS (disorder)"@en
"Disturbance of sulphur-bearing amino-acid metabolism NOS"@en
"Disturbances of sulphur-bearing amino-acid metabolism"@en
"Sulphuraminoacidaemia"@en
"inborn disorder of methionine cycle and sulfur amino acid metabolism"@en
"obsolete sulfuraminoacidemia"@en
schema:description
"Human disease"@en
schema:dateModified "2026-10-24T00:34:54+00:00"^^xsd:dateTime
schema:version 2560167040
wikibase:identifiers 10
wikibase:sitelinks 0
wikibase:statements 37
p:P14914 wd:statement/Q19001322-FFB2CAAA-9AA7-425A-A4F0-21DB540F876A
p:P1550 wd:statement/Q19001322-F7ABDB48-D82E-4880-BD92-0305131A3164
p:P2293 wd:statement/Q19001322-1C4C41C7-789C-4B2B-8578-A26592EADF42
wd:statement/Q19001322-29859429-D77F-473A-AC3E-EADC27DD42F0
wd:statement/Q19001322-31ED9589-B696-4500-8AAF-F5D767BD604E
wd:statement/Q19001322-47FD7BBE-A088-402B-B43D-61AF4364BC1F
wd:statement/Q19001322-513C9DAE-410A-48F6-93A1-01FA077518A2
wd:statement/Q19001322-66257E24-7C6C-4C14-B945-51C66438D64E
wd:statement/Q19001322-665951A6-6A1C-4D79-B9F8-0A3A1D4565AE
wd:statement/Q19001322-74D31D8F-D886-45B8-B3DD-65F247389B84
wd:statement/Q19001322-7CB7B99C-432E-4F1D-83DE-75CEA8983D99
wd:statement/Q19001322-8BE405E3-BE0A-48D5-A019-22EAB2BBF3AC
wd:statement/Q19001322-8D12E9C1-52E1-4AA2-ACF8-D6172A0585C7
wd:statement/Q19001322-9C1CDF55-6155-4E62-BA28-913E5C8E6556
wd:statement/Q19001322-9C69A4F0-ED21-4C8A-97EC-540DE67AF243
wd:statement/Q19001322-ABF8E046-F2B3-4E2F-959B-46A8E9407CB1
wd:statement/Q19001322-C3CE297D-FE0A-430B-9C8C-1AE947DA11B1
wd:statement/Q19001322-D9C4D95F-5ECF-4611-8C64-CEC0B266B495
wd:statement/Q19001322-DF17B12A-FA19-4A61-98A5-E6D5FFEE4BEE
wd:statement/Q19001322-E76B883C-C689-4051-84A0-74CC2FF7FE95
wd:statement/Q19001322-EC77E3D5-37D4-409F-B06F-1DD5B882B63A
wd:statement/Q19001322-EFC441C4-E6A4-40BB-BD8B-EE178C02BAB8
wd:statement/Q19001322-FF412A2B-CB99-467C-8CD2-5FAD6A240993
p:P279 wd:statement/Q19001322-d683bae8-41c4-5c3b-cdbc-dd6936105e2b
p:P2888 wd:statement/Q19001322-02F46658-E276-4755-8393-8A196292C0AB
wd:statement/Q19001322-074DD8F1-670A-4BD9-B84A-C7DC48F71A3C
wd:statement/Q19001322-D1FDE94D-5E81-456B-8F05-ED66DF5D95CB
p:P2892 wd:statement/Q19001322-784E3058-08AD-4C16-9623-1868AE6F7AC4
wd:statement/Q19001322-feb1a60f-4dc1-03d5-af1d-a9f19523cf82
p:P31 wd:statement/Q19001322-CB500F9C-0227-4229-BC83-0558111E28EC
p:P3201 wd:statement/Q19001322-26786335-E376-4B05-A509-C9DE71FD293B
p:P4229 wd:statement/Q19001322-699DCBE1-709E-44B0-89E6-87C184E3640E
p:P493 wd:statement/Q19001322-CD552D41-6FB2-42C7-9226-6F1D49E98C0E
p:P494 wd:statement/Q19001322-f82f734a-4dd3-919b-78db-46ce3da70cb7
p:P5008 wd:statement/Q19001322-FC0085A5-6515-43C5-8985-C4BB9A8BFC2F
p:P5270 wd:statement/Q19001322-6FDE78E0-E374-4F43-B2AD-38FF91FF5574
p:P699 wd:statement/Q19001322-F3EAECE4-B4FC-4AF1-A499-8A124CA5F325
p:direct-normalized/P3201 <http://purl.bioontology.org/ontology/MDRFRE/10001938>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0019222>
wdt:P14914 "D79173"
wdt:P1550 "79173"
wdt:P2293 MTHFR
MTR
CBS
SUOX
HCFC1
MAT1A
MOCS1
MOCS2
MTRR
PRDX1
ABCD4
SELENBP1
GPHN
MMACHC
GNMT
MMADHC
LMBRD1
THAP11
ADK
AHCY
CTH
wdt:P279 amino acid metabolic disorder
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_79173>
wdt:P2892 "C0268613"
"C5680126"
wdt:P31 type of disease
wdt:P3201 "10001938"
wdt:P4229 "E72.1"
wdt:P493 "270.4"
wdt:P494 "E72.1"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0019222"
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data from SPARQL profile: Wikidata