ORPHA:98374

Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder

Synonyms: Hemolytic anemia due to an erythroenzymopathy

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	Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder	Hemolytic anemia due to an erythroenzymopathy
fr	Anémie hémolytique par anomalie du métabolisme nucléotidique de l'érythrocyte	Anémie hémolytique par erythroenzymopathie
de	Hämolytische Anämie durch Erythrozyten-Nukleotidstoffwechselstörung	Hämolytische Anämie durch Erythroenzymopathie
es	Anemia hemolítica por trastorno del metabolismo nucleotídico de los eritrocitos	Anemia hemolítica por una eritroenzimopatía
it	Anemia emolitica da difetto del metabolismo nucleotidico degli eritrociti	Anemia emolitica da eritroenzimopatia
nl	Hemolytische anemie als gevolg van een erytrocytnucleotidestofwisselingsstoornis	Hemolytische anemie als gevolg van een erytro-enzymopathie
pt	Doença do metabolismo nucleotídico dos eritrócitos
pl	Niedokrwistość hemolityczna z powodu zaburzeń metabolizmu nukleotydów w erytrocytach	Niedokrwistość hemolityczna z powodu erytroenzymopatii
cs	Hemolytická anémie způsobená poruchou metabolismu nukleotidů erytrocytu	Hemolytická anémie způsobená enzymopatií erytrocytů
uk	Гемолітична анемія внаслідок порушення нуклеотидного обміну еритроцитів	Гемолітична анемія внаслідок еритроензимопатії
zh	红细胞核苷酸代谢紊乱所致溶血性贫血	红细胞酶病所致溶血性贫血
tr	Eritrosit nükleotid metabolizması bozukluğuna bağlı hemolitik anemi	Eritroenzimopatiye bağlı hemolitik anemi

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	D55.3	E	specific	validated
ICD-11	3A10.Y	NTBT	index	validated
UMLS	C5680359	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:98369Rare constitutional hemolytic anemia due to an enzyme disorder
rare genetic diseases; rare hematological diseases

Children (3):

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/98374
This record as JSON: /data/d/98374.json