Hypertension
Basic details
Preferred term: Hypertension
Alt. terms: high blood pressure | Systemic hypertension | primary hypertension
HPO term: Hypertension
HPO code: HP:0000822
GenIA ID: 81
Last updated on: 2024-04-25 14:48:58
Cross ref. with other ontologies
NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: I10
Description
The presence of chronic increased pressure in the systemic arterial system.
Hierarchical classification
Reported patients added to GenIA DB
SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
---|---|---|---|---|---|---|---|
101017 | F | 210232 | 54 | German | Hypertension | PMID:34975878 [Fam.F003:P003] | |
101022 | M | 210482 | 19 | German | Hypertension | PMID:34975878 [Fam.F007:P007] | |
101038 | F | 210182![]() |
- | Caucasian | Hypertension | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:25329329 [Fam.B:II.6(B.II.4)]; PMID:30250467 [B.II.4]; PMID:29729943 [Fam.B:II.6(B.II.4 (16))]; PMID:34975878 [Fam.F014:III.6(P015)]; PMID:27418640 [P14(5)] |
101078 | F | 211301 | 53 | Hypertension | PMID:34975878 [Fam.F044:P044] | ||
101088 | M | 211560 | 44 | German | Hypertension | PMID:34975878 [Fam.F054:P054] | |
101125 | M | 210429 | 40 | German | Hypertension | Immunodeficiency, common variable, 1 | PMID:34975878 [Fam.F076:P076]; PMID:35486341 [P060] |
101134 | F | 210901 | 36 | Hypertension | PMID:34975878 [Fam.F083:P083] | ||
101153 | M | 210757 | 38 | German | Hypertension | Hyper-IgE recurrent infection syndrome 2 | PMID:34390440 [HIES55] |
101167 | M | 211470![]() |
- | Hypertension | NFKB1 insufficiency | PMID:34975878 [Fam.F108:P108]; PMID:33486103 [Fam.1:II.1(patient)]; PMID:150198 [Fam.DT:II.1(510)] | |
101186 | F | 211471 | - | Hypertension | PMID:34975878 [Fam.F118:P118] | ||
101207 | F | 211502 | 63 | Hypertension | PMID:34975878 [Fam.F130:P130] | ||
101410 | F | 210902 | - | German | Hypertension | Adenosine deaminase 2 deficiency | PMID:34975878 [Fam.F141:P141]; PMID:28493328 [P4] |
101476 | F | 210512 | - | Hypertension | PMID:34975878 [Fam.F158:P158] | ||
101537 | M | 210949 | 51 | Hypertension | PMID:34975878 [Fam.F178:P178] | ||
101579 | F | 210773 | - | Turkish | Hypertension | Adenosine deaminase 2 deficiency | PMID:28493328 [P1]; PMID:31857261 [Patient 13] |
101617 | M | 210994 | 53 | Hypertension | Immunodeficiency, common variable, 2 | PMID:34975878 [Fam.F212:P212] | |
101798 | M | 211117 | - | Hypertension | Adenosine deaminase 2 deficiency | PMID:28493328 [P11] | |
101819 | F | 211386 | - | Hypertension | Immunodeficiency, common variable, 2 | PMID:31057532 [Fam.F:I.2] | |
102933 | M | 215034 | - | Hypertension | T-cell lymphopenia with or without nail dystrophy, AD | PMID:31447097 [P22]; PMID:37419334 [P22(22)] | |
103006 | M | 215081![]() |
- | North American | Hypertension | PMID:23861857 [Fam.Patient:I.1] | |
103351 | M | 215121![]() |
- | North American | Hypertension | Deafness 1, with or without thrombocytopenia | PMID:32594080 [P1(III.1)] |
103723 | M | 215232![]() |
0 | Georgian Jewish | Hypertension | Adenosine deaminase 2 deficiency | PMID:24552285 [Fam.A:III.1(A-III-1)] |
103732 | M | 215232![]() |
3 | Georgian Jewish | Hypertension | Adenosine deaminase 2 deficiency | PMID:24552285 [Fam.A:III.4(A-III-4)] |
103773 | F | 215236![]() |
- | Georgian Jewish | Renal Hypertension | Adenosine deaminase 2 deficiency | PMID:24552285 [Fam.E:II.2(E-II-2)] |
103776 | F | 215237![]() |
1 | German | Hypertension | Adenosine deaminase 2 deficiency | PMID:24552285 [Fam.F:II.1(F-II-1)] |
103783 | F | 215238 | 28 | Georgian Jewish | Hypertension | Adenosine deaminase 2 deficiency | PMID:24552285 [S-1] |
103785 | M | 215240 | - | Georgian Jewish | Hypertension | Adenosine deaminase 2 deficiency | PMID:24552285 [S-3] |
103786 | M | 215241 | 10 | Turkish | Hypertension | Adenosine deaminase 2 deficiency | PMID:24552285 [T-1] |
103827 | M | 215255![]() |
6 | Pakistani | Hypertension | Adenosine deaminase 2 deficiency | PMID:25278816 [Fam.F750:II.1(P2)] |
104286 | F | 215445![]() |
- | Dutch | Hypertension | Hyper-IgE recurrent infection syndrome 1 | PMID:19878510 [Fam.1:III.3(V3)]; PMID:12572706 [Fam.1:III.4(III.3)] |
105339 | F | 215701![]() |
- | Pakistani | Hypertension | Immunodeficiency 87 | PMID:31308374 [Fam.A:III.4(P1)] |
105761 | F | 215851![]() |
- | Finnish | Hypertension | Immunodeficiency, common variable, 14 | PMID:34451894 [Fam.Patient:II.1(sister)]; PMID:37876937 [Fam.C:II.1(C.2)] |
106422 | F | 216014 | - | Hypertension | NFKB1 insufficiency | PMID:150198 [Fam.DX:541]; PMID:34447408 [1(I.1)] | |
106577 | F | 216081![]() |
- | Caucasian | Hypertension | Adenosine deaminase 2 deficiency | PMID:26867732 [Fam.D:II.2(P6)] |
106684 | F | 216108 | 67 | Asian | Hypertension | NFKB1 insufficiency | PMID:36105815 [G136S] |
106861 | F | 216175 | - | Caucasian | Hypertension | Adenosine deaminase 2 deficiency | PMID:31008556 [Fam.7:P9] |
106868 | M | 216177 | - | Japanese | Hypertension | Adenosine deaminase 2 deficiency | PMID:33529688 [Fam.2:II.2(P3)] |
106875 | F | 216179 | - | Japanese | Hypertension | Adenosine deaminase 2 deficiency | PMID:33529688 [Fam.4:II.3(P6)] |
106884 | F | 216181 | 12,- | Japanese | Hypertension,Renal Hypertension | Adenosine deaminase 2 deficiency | PMID:33529688 [Fam.6:II.2(P8)] |
107217 | M | 216376 | - | Caucasian | Hypertension | Adenosine deaminase 2 deficiency | PMID:27059682 [D] |
107218 | F | 216377 | - | Caucasian | Hypertension | Adenosine deaminase 2 deficiency | PMID:27059682 [E] |
107219 | F | 216378 | - | Caucasian | Hypertension | Adenosine deaminase 2 deficiency | PMID:27059682 [F] |
107224 | F | 216380 | 17 | Singaporean | Hypertension | Adenosine deaminase 2 deficiency | PMID:27069017 [Patient] |
*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).