ORPHA:447874

Biological anomaly without phenotypic characterization

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	Biological anomaly without phenotypic characterization
fr	Anomalie biologique sans caractérisation phenotypique
de	Biologische Anomalie ohne phänotypische Charakterisierung
es	Anomalías biológicas sin caracterización fenotípica
it	Anomalia biologica senza caratterizzazione fenotipica
nl	Biologische anomalie zonder fenotypische karakterisering
pt	Anomalia biológica sem caracterização fenotípica
pl	Anomalie biologiczne bez charakterystyki fenotypowej
cs	Biologická anomálie bez fenotypové charakterizace
uk	Біологічна аномалія без фенотипової характеристики
zh	无临床表型的生物学指标异常
tr	Fenotipik karakterizasyon göstermeyen biyolojik anomali

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	18652	E		validated
UMLS	C5681202	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:98053Rare genetic disease

Parents in the classifications (1):

ORPHA:98053Rare genetic disease
rare genetic diseases

Children (5):

Codes that Orphanet moved or referred to this one:

ORPHA:93594OBSOLETE: Alpha-1-antichymotrypsin deficiency referred to · inactive

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/447874
This record as JSON: /data/d/447874.json