ORPHA:289877

Transient hyperammonemia of the newborn

Orphadata ships no English definition for this code.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Transient hyperammonemia of the newborn
fr	Hyperammoniémie transitoire du nouveau-né
de	Transiente Hyperammonämie des Neugeborenen
es	Hiperamonemia transitoria del recién nacido
it	Iperammoniemia transitoria neonatale
nl	Transiënte hyperammoniëmie van neonaat
pt	Hiperamonémia transitória do recém-nascido
pl	Przejściowa hiperammonemia noworodków
cs	Přechodná hyperamonemie novorozenců
uk	Транзиторна гіперамоніємія новонароджених
zh	新生儿一过性高氨血症
tr	Yenidoğan geçici hiperamonyemisi

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	P74.8	NTBT	attributed	validated
ICD-11	5C50.AY	NTBT	index	validated
MONDO	0017357	E		validated
UMLS	C0268549	E		validated

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

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

ORPHA:91088Other metabolic disease
rare inborn errors of metabolism; rare genetic diseases

No children.

0 direct

Orphanet records no gene directly on this code.

1 record

Type	Class	Value	Area	Qualification	Validation	Source
Point prevalence	Unknown	—	Worldwide	Class only	Not yet validated	ORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

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