ORPHA:248358

Rare thrombotic disorder due to a coagulation factors defect

Type: Category
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Rare thrombotic disorder due to a coagulation factors defect
fr	Maladie thrombotique rare par déficit en facteurs de coagulation
de	Seltene thrombotische Störung durch Gerinnungsfaktoren-Defekt
es	Enfermedad trombótica rara por un defecto de factores de coagulación
it	Disturbo trombotico raro da difetto dei fattori di coagulazione
nl	Zeldzame trombotische stoornis als gevolg van een coagulatiefactordefect
pt	Doença trombótica rara por defeito nos fatores de coagulação
pl	Rzadkie zaburzenie krzepnięcia z powodu defektu czynników krzepnięcia
cs	Vzácné trombotické poruchy způsobené defektem koagulačních faktorů
uk	Рідкісний тромботичний розлад, зумовлений дефектом факторів згортання крові
zh	凝血因子缺陷所致罕见性血栓性疾病
tr	Pıhtılaşma faktörleri defektine bağlı nadir trombotik bozukluk

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	16632	E		validated
UMLS	C5680692	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97992Rare hematologic disease

Parents in the classifications (1):

ORPHA:182054Rare thrombotic disease of hematologic origin
rare hematological diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/248358
This record as JSON: /data/d/248358.json