SHMARQL

glucocorticoid-remediable aldosteronism

<http://www.wikidata.org/entity/Q17149181>

Human disease
rdfs:label
"glucocorticoid-remediable aldosteronism"@en
skos:altLabel
"Acth-Dependent Hyperaldosteronism Syndrome"@en
"Aldosteronism, Sensitive to Dexamethasone"@en
"Dexamethasone sensitive hypertension"@en
"Dexamethasone-sensitive hypertension"@en
"FH-I"@en
"FH1"@en
"Familial hyperaldosteronism type 1"@en
"Familial hyperaldosteronism type I"@en
"Fh 1"@en
"GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM; GRA"@en
"GRA"@en
"Glucocorticoid remediable aldosteronism"@en
"Glucocorticoid sensitive hypertension"@en
"Glucocorticoid-Suppressible Hyperaldosteronism"@en
"Glucocorticoid-remediable aldosteronism"@en
"Glucocorticoid-sensitive hypertension"@en
"Hyperaldosteronism, Familial, Type 1"@en
"Hyperaldosteronism, familial type 1"@en
schema:description
"Human disease"@en
schema:dateModified "2026-10-24T00:16:14+00:00"^^xsd:dateTime
schema:version 2560164107
wikibase:identifiers 14
16
wikibase:sitelinks 2
wikibase:statements 45
p:P11430 wd:statement/Q17149181-09456ec5-4232-6a95-b917-0b1dd6d11f26
p:P14914 wd:statement/Q17149181-80FF71D1-E97D-4812-9B5B-577DA2933E50
p:P1550 wd:statement/Q17149181-DAAAA43F-4164-4E53-949C-0F058A32142B
p:P1692 wd:statement/Q17149181-31AB7B61-0D8E-4609-988C-F781D43CB8B8
p:P1748 wd:statement/Q17149181-54BD90A2-3730-4DFE-B022-FECDC4CB82CE
p:P1995 wd:statement/Q17149181-036F77D0-F80C-4BF0-B15C-F80ED8D07FF8
p:P2293 wd:statement/Q17149181-3A9A5220-EF5F-4055-B021-951A2C0B81FC
wd:statement/Q17149181-D69DC354-750E-4E93-A3F6-C17F753C2023
p:P279 wd:statement/Q17149181-36fe523d-42a8-46be-2c7b-529d52c39333
wd:statement/Q17149181-3BEA984C-4621-4349-830F-7BB72F9C636A
wd:statement/Q17149181-982380eb-4ee5-3040-7751-7f9f025d80ba
p:P2841 wd:statement/Q17149181-4D13197A-C391-43C0-BF54-C1E2F995C43B
wd:statement/Q17149181-C84C6503-5E0D-45E1-8D7C-4B67B1E14C2E
wd:statement/Q17149181-D10E8214-8C1B-4A42-BDE0-604D56AC8FCB
p:P2888 wd:statement/Q17149181-0E203D0C-5E40-4074-8CF1-A259EA8C72A0
wd:statement/Q17149181-CA9ED413-B405-450D-849A-6BB91E0D3D3C
wd:statement/Q17149181-CF3A4454-0406-40E8-A8F9-5E17DE54C0FA
p:P2892 wd:statement/Q17149181-00D83065-67FD-41BC-93A1-EFFEF3864BDB
wd:statement/Q17149181-D3D2B7BB-C32C-4EBE-A2B0-92C9F689D390
p:P31 wd:statement/Q17149181-919B55D4-3433-45F2-BFF6-C27B0C7FBB79
wd:statement/Q17149181-E32AE2F6-38C6-4A95-ACAD-F93BCABBC802
p:P4229 wd:statement/Q17149181-A30958E8-E087-4606-A99E-0D2004FB09AF
wd:statement/Q17149181-D1A10073-8DB5-46E5-BE1F-06EB6FA00CC6
p:P4317 wd:statement/Q17149181-6A5943B9-6A57-44B4-8951-ED48B634C6E1
p:P486 wd:statement/Q17149181-54CB7FE2-D231-45B1-AA08-84AC95A17169
p:P492 wd:statement/Q17149181-63F26CAD-75B7-4AA7-8309-E3586785FFB0
p:P5008 wd:statement/Q17149181-771CD595-7950-4818-B303-3CE98727DBC0
p:P5270 wd:statement/Q17149181-04F45A12-A878-4E83-9F04-0A3F40357215
p:P6366 wd:statement/Q17149181-56000147-012A-4E70-A607-60FF7A852A90
p:P6532 wd:statement/Q17149181-060659CA-5182-429B-A3DF-1E021A9772A7
wd:statement/Q17149181-0A9BDD71-00AF-41BB-AEA7-626B9B4C4310
wd:statement/Q17149181-1E1ADFF5-47C9-40AD-BCF3-417742AC6AA5
wd:statement/Q17149181-22A4E7F9-556D-4D0F-86DB-0DBCBF846105
wd:statement/Q17149181-2D4661B9-B5F6-4462-8508-0F30EA2655DF
wd:statement/Q17149181-3A343B2E-FF4E-42DD-89EE-65BFECD0BA97
wd:statement/Q17149181-46425103-8D8D-47DC-BCC4-22E934637D30
wd:statement/Q17149181-48D9F263-7C15-45F0-8CB4-15FB6E567520
wd:statement/Q17149181-7C999A98-5AD9-4024-B4C9-AFF02B40988D
wd:statement/Q17149181-D2093A89-C8A5-4611-9BEE-8F72BA1A1342
wd:statement/Q17149181-D46E2127-4832-45C2-BE17-1B34C2ADB75D
wd:statement/Q17149181-D986FA86-B94E-46ED-9FF0-553EE46B9063
wd:statement/Q17149181-E5316737-6736-4C79-8E68-653A244473A5
p:P665 wd:statement/Q17149181-2F3DFA24-6765-4161-A7A2-68CE95AA35B7
p:P699 wd:statement/Q17149181-02F451F7-159B-4C2C-97AE-4206C7A64F4D
p:P7807 wd:statement/Q17149181-78c60f33-466d-d999-6943-a094f5a252c9
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C563177>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0007080>
p:direct-normalized/P6366 <https://makg.org/entity/2781129315>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00602>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:14080>
wdt:P11430 "DI-02693"
wdt:P14914 "D00403"
wdt:P1550 "403"
wdt:P1692 "255.11"
wdt:P1748 "C123248"
wdt:P1995 endocrinology
wdt:P2293 CYP11B2
CYP11B1
wdt:P279 Familial hyperaldosteronism
genetic hypertension
wdt:P2841 childhood onset
juvenile onset
adult onset
wdt:P2888 <http://identifiers.org/doid/DOID:14080>
<http://purl.obolibrary.org/obo/DOID_14080>
<http://www.orpha.net/ORDO/Orphanet_403>
wdt:P2892 "C1260386"
"C3838731"
wdt:P31 type of disease
rare disease
wdt:P4229 "E26.0"
"E26.02"
wdt:P4317 "2790"
wdt:P486 "C563177"
wdt:P492 "103900"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0007080"
wdt:P6366 "2781129315"
wdt:P6532 Abnormal circulating renin
Secretory adrenocortical adenoma
nausea
tinnitus
nosebleed
cesarean section
muscle weakness
congenital adrenal hyperplasia
arterial hypertension
intracranial hemorrhage
polydipsia
hypokalemia
headache
wdt:P665 "H00602"
wdt:P699 "DOID:14080"
wdt:P7807 "1994802431"
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