ORPHA:101985

Quantitative and/or qualitative congenital phagocyte 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	Quantitative and/or qualitative congenital phagocyte defect
fr	Défaut congénital quantitatif et/ou qualitatif des phagocytes
de	Phagozytendefekt, kongenitaler (Funktion und/oder Anzahl)
es	Defectos congénitos en el número, función o ambos aspectos de los fagocitos
it	Difetti congeniti del numero e/o della funzione dei fagociti
nl	Kwantitatief en/of kwalitatief congenitaal fagocytdefect
pt	Deficiência da função dos fagócitos
pl	Wrodzone zaburzenia liczby i/lub funkcji fagocytów
cs	Kvantitativní a/nebo kvalitativní vrozený defekt fagocytů
uk	Кількісний та/або якісний вроджений дефект фагоцитів
zh	定量和/或定性先天性吞噬细胞缺陷
tr	Kantitatif ve / veya kalitatif doğumsal fagosit defekti

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	Validation
MONDO	15133	E	validated
UMLS	C5681777	E	validated
GARD	19808	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:98004Rare immune disease

Parents in the classifications (1):

ORPHA:101988Primary immunodeficiency due to a defect in innate immunity
rare genetic diseases; rare immunological 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/101985
This record as JSON: /data/d/101985.json