ORPHA:238699

Transient congenital hypothyroidism due to neonatal factor

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	Transient congenital hypothyroidism due to neonatal factor
fr	Hypothyroïdie congénital transitoire de cause néonatale
de	Hypothyreose, kongenitale transiente, durch neonatalen Faktor
es	Hipotiroidismo congénito transitorio por un factor neonatal
it	Ipotiroidismo congenito transitorio di origine neonatale
nl	Tijdelijke congenitale hypothyreoïdie als gevolg van neonatale factor
pt	Hipotiroidismo transitório congénito por fator neonatal
pl	Przejściowa wrodzona niedoczynność tarczycy z powodu czynnika noworodkowego
cs	Tranzientní vrozená hypotyreóza způsobená faktorem ze strany novorozence
uk	Транзиторний вроджений гіпотиреоз внаслідок неонатального фактору
zh	新生儿因素所致短暂性先天性甲状腺功能减退
tr	Yenidoğan faktörüne bağlı geçici doğumsal hipotiroidi

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	P72.2	E	specific	validated
MONDO	0016556	E		validated
MONDO	16556	E		validated
UMLS	C5680930	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:97978Rare endocrine disease

Parents in the classifications (1):

ORPHA:178045Transient congenital hypothyroidism
rare endocrine 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/238699
This record as JSON: /data/d/238699.json