raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:220443

OBSOLETE: Bleeding diathesis due to thromboxane synthesis deficiency

inactive · referred to ORPHA:728656Bleeding diathesis due to thromboxane A2 receptor variants

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete with resources

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Bleeding diathesis due to thromboxane A2 receptor variants

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Bleeding diathesis due to thromboxane synthesis deficiency
frOBSOLETE : Troubles hémorragiques par déficit de synthèse de la thromboxane
deOBSOLET: Hämorrhagische Diathese durch Thromboxan-Synthetase-MangelOBSOLET: Thromboxan-Synthetase-Mangel
esOBSOLETO: Diátesis hemorrágica por deficiencia de síntesis de tromboxano
itOBSOLETO: Diatesi emorragica da deficit della sintesi del trombossano
nlOBSOLEET: Bloedingsdiathese door deficiëntie van thromboxaansynthese
ptOBSOLETO: Diátese hemorrágica por deficiência na síntese de tromboxano
plNIEAKTUALNE: Skaza krwotoczna z powodu niedoboru syntezy tromboksanu
csNEAKTUÁLNÍ: Hemoragická diatéza způsobená deficitem syntézy tromboxanu
ukКровоточивий діатез внаслідок дефіциту синтезу тромбоксану
zh血栓烷合成缺陷所致出血素质
trTromboksan sentez eksikliğine bağlı kanama diyatezi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card