ORPHA:506207

Rare disorder potentially indicated for transplant

Type: Category
Group: Group of disorders
Status: active

A group of rare disorders with irreversible organ and/or system dysfunction(s), or the effects of dysfunction after alternative medical and surgical treatments have been utilized, for which the benefits of transplantation outweigh the risk of continuing alternative modalities.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Rare disorder potentially indicated for transplant
fr	Maladie rare possiblement indiquée pour une transplantation
de	Seltene Krankheit zur potentiellen Transplantation indiziert
es	Trastorno raro potencialmente indicado para trasplante
it	Malattia rara con potenziale indicazione al trapianto
nl	Zeldzame aandoening mogelijk geïndiceerd voor transplantatie
pt	Doença rara com potencial indicação para transplante
pl	Rzadka choroba, będąca potencjalnym wskazaniem do przeszczepu
cs	Vzácná porucha indikovaná k transplantaci
uk	Рідкісне захворювання, що є потенційним показанням для трансплантації
zh	可能需要移植的罕见疾病
tr	Organ nakli gerektirebilen nadir hastalık

Definition in:

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5681217	E		validated

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

Classification

Parents in the classifications (1):

ORPHA:565779Rare disorder potentially indicated for transplant or complication after transplantation
rare transplant-related disorders

Children (6):

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/506207
This record as JSON: /data/d/506207.json